Tag: 169.6314

Lu, Dong-Dong et al. published their research in Journal of Organic Chemistry in 2017 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 615-20-3

Bulky Yet Flexible Pd-PEPPSI-IPentAn for the Synthesis of Sterically Hindered Biaryls in Air was written by Lu, Dong-Dong;He, Xu-Xian;Liu, Feng-Shou. And the article was included in Journal of Organic Chemistry in 2017.Recommanded Product: 615-20-3 This article mentions the following:

In this report, a type of moisture and air stable Pd-PEPPSI-IPentAn complex with the combination of acenaphthyl on the backbone and isopentyl groups on N-aryl moieties, I, was described and applied in the Suzuki-Miyaura cross-coupling reaction in air. The reaction conditions were optimized, and the structure-reactivity relationships between I and other classical efficient Pd-PEPPSI complexes were investigated intensively. Our study demonstrated that both the backbone and N-aryl moieties gave rise to a significant effect on this transformation when exposed to air. A wide range of sterically hindered (hetero)aryl chlorides with (hetero)arylboronic acids were compatible, giving good to excellent isolated yields of sterically hindered bi(hetero)aryls. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3Recommanded Product: 615-20-3).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 615-20-3

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Lu, Dong-Dong et al. published their research in Journal of Organic Chemistry in 2017 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 615-20-3

Bulky Yet Flexible Pd-PEPPSI-IPentAn for the Synthesis of Sterically Hindered Biaryls in Air was written by Lu, Dong-Dong;He, Xu-Xian;Liu, Feng-Shou. And the article was included in Journal of Organic Chemistry in 2017.Recommanded Product: 615-20-3 This article mentions the following:

In this report, a type of moisture and air stable Pd-PEPPSI-IPentAn complex with the combination of acenaphthyl on the backbone and isopentyl groups on N-aryl moieties, I, was described and applied in the Suzuki-Miyaura cross-coupling reaction in air. The reaction conditions were optimized, and the structure-reactivity relationships between I and other classical efficient Pd-PEPPSI complexes were investigated intensively. Our study demonstrated that both the backbone and N-aryl moieties gave rise to a significant effect on this transformation when exposed to air. A wide range of sterically hindered (hetero)aryl chlorides with (hetero)arylboronic acids were compatible, giving good to excellent isolated yields of sterically hindered bi(hetero)aryls. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3Recommanded Product: 615-20-3).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 615-20-3

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Jafari, Behzad et al. published their research in ChemistrySelect in 2019 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. The thiazole ring has been identified as a central feature of numerous natural products, perhaps the most famous example of which is epothilone. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 2-Chlorobenzothiazole

Synthesis of 2-Alkynyl- and 2-Amino-12H-benzothiazolo[2,3-b]quinazolin-12-ones and Their Inhibitory Potential against Monoamine Oxidase A and B was written by Jafari, Behzad;Jalil, Saquib;Zaib, Sumera;Safarov, Sayfidin;Khalikova, Muattar;Khalikov, Djurabay;Ospanov, Meirambek;Yelibayeva, Nazym;Zhumagalieva, Shynar;Abilov, Zharylkasyn A.;Turmukhanova, Mirgul Z.;Kalugin, Sergey N.;Salman, Ghazwan Ali;Ehlers, Peter;Hameed, Abdul;Iqbal, Jamshed;Langer, Peter. And the article was included in ChemistrySelect in 2019.Recommanded Product: 2-Chlorobenzothiazole This article mentions the following:

The 2-alkynyl- and 2-aminobenzothiazolo[2,3-b]quinazolin-12-ones I (R = isopropylaminyl, diphenylaminyl, morpholin-4-yl, etc.) and II (Ar = Ph, 4-tert-butylphenyl, naphthalen-1-yl, etc.) have been synthesized by Palladium catalyzed Buchwald-Hartwig and Sonogashira reactions. Synthesized derivatives were further evaluated for their role as potential inhibitors of monoamine oxidase A and B (MAO-A and B) isoenzymes. Most compounds possess moderate to excellent inhibitory potential against MAO-A and MAO-B. The 2-amino-substituted derivatives show a significantly higher activity as compared to 2-alkynyl- and previously reported 2-aryl derivatives Studied compounds might be employed as novel monoamine oxidase inhibitors and may provide insights for the development of new drug candidates against neurol. diseases. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3Recommanded Product: 2-Chlorobenzothiazole).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. The thiazole ring has been identified as a central feature of numerous natural products, perhaps the most famous example of which is epothilone. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 2-Chlorobenzothiazole

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Kunkle, Trent et al. published their research in Journal of Medicinal Chemistry in 2018 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. There are numerous natural products that possess a thiazole ring with broad pharmacological activities. Thiamine, also known as vitamin B1, possesses a thiazole ring linked with 2-methylpyrimidine-4-amine as hydrochloride salt.Computed Properties of C7H4ClNS

Hydroxybiphenylamide GroEL/ES inhibitors are potent antibacterials against planktonic and biofilm forms of Staphylococcus aureus was written by Kunkle, Trent;Abdeen, Sanofar;Salim, Nilshad;Ray, Anne-Marie;Stevens, Mckayla;Ambrose, Andrew J.;Victorino, Jose;Park, Yangshin;Hoang, Quyen Q.;Chapman, Eli;Johnson, Steven M.. And the article was included in Journal of Medicinal Chemistry in 2018.Computed Properties of C7H4ClNS This article mentions the following:

We recently reported the identification of a GroEL/ES inhibitor (1, N-(4-(benzo[d]thiazol-2-ylthio)-3-chlorophenyl)-3,5-dibromo-2-hydroxybenzamide) that exhibited in vitro antibacterial effects against Staphylococcus aureus comparable to vancomycin, an antibiotic of last resort. To follow up, we have synthesized 43 compound 1 analogs to determine the most effective functional groups of the scaffold for inhibiting GroEL/ES and killing bacteria. Our results identified that the benzothiazole and hydroxyl groups are important for inhibiting GroEL/ES-mediated folding functions, with the hydroxyl essential for antibacterial effects. Several analogs exhibited >50-fold selectivity indexes between antibacterial efficacy and cytotoxicity to human liver and kidney cells in cell culture. We found that MRSA was not able to easily generate acute resistance to lead inhibitors in a gain-of-resistance assay and that lead inhibitors were able to permeate through established S. aureus biofilms and maintain their bactericidal effects. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3Computed Properties of C7H4ClNS).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. There are numerous natural products that possess a thiazole ring with broad pharmacological activities. Thiamine, also known as vitamin B1, possesses a thiazole ring linked with 2-methylpyrimidine-4-amine as hydrochloride salt.Computed Properties of C7H4ClNS

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Chen, Yuqian et al. published their research in Journal of Solid State Chemistry in 2021 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. The thiazole ring is notable as a component of the vitamin thiamine (B1). Electrophilic attack at nitrogen depends on the presence of electron density at nitrogen as well as the position and nature of substituent linked to the thiazole ring.HPLC of Formula: 615-20-3

One-dimensional La(III) coordination polymer displaying multi-responsive luminescence activities towards Fe3+, acetone and benzothiozoles was written by Chen, Yuqian;Xian, Guoxuan;Yan, Hui;Wang, Yuhao;Li, Yunwu;Lu, Jing;Xu, Haijun;Tao, Jiayu;Wang, Suna. And the article was included in Journal of Solid State Chemistry in 2021.HPLC of Formula: 615-20-3 This article mentions the following:

Through reaction of La(NO3)3 with a flexible carboxylic acid ligand named 3,5-bis[(2-carboxyphenyl)oxy]benzoic acid (H3L) under solvothermal condition, the complex with the formula of [La(L)(DMF)2] (1) was obtained. One-dimensional chain of the complex was generated through the connection of binuclear units of La2(COO)4 across the flexible acid ligands. Luminescence results showed that different pollutants (Fe3+, acetone and benzothiophene organic compounds) could quench the luminescence of the blue emission of the complex in DMF with much low detection limit. Among several 2-substituted benzothiophene compounds, 2,2鈥?dithiobisbenzothiazole (DM) has a strongest binding constant of 10.8 x 104 M-1 and lowest detection limit of 0.332 渭M (0.110 ppm). All quenching effect was found within 15 s. The sensing mechanism was investigated through a series of experiments and theor. calculation Complex 1 could be employed as a multi-responsive chemosensor for detection of different pollutants with high sensitivity and fast response. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3HPLC of Formula: 615-20-3).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. The thiazole ring is notable as a component of the vitamin thiamine (B1). Electrophilic attack at nitrogen depends on the presence of electron density at nitrogen as well as the position and nature of substituent linked to the thiazole ring.HPLC of Formula: 615-20-3

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Pilathottathil, Fathima et al. published their research in Journal of Organic Chemistry in 2022 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles are a class of five-membered rings containing nitrogen and sulfur with excellent antitumor, antiviral and antibiotic activities. Electrophilic attack at nitrogen depends on the presence of electron density at nitrogen as well as the position and nature of substituent linked to the thiazole ring.Quality Control of 2-Chlorobenzothiazole

Heteroarylation of Sulfenate Ions In Situ Generated from 尾-Sulfinyl Esters under Transition-Metal-Free Conditions was written by Pilathottathil, Fathima;Unnikrishnan, Sreelakshmi;Kaliyamoorthy, Alagiri. And the article was included in Journal of Organic Chemistry in 2022.Quality Control of 2-Chlorobenzothiazole This article mentions the following:

Heteroaryl sulfoxides are an integral part of several bioactive mols. and pharmaceuticals. A transition-metal-free route for the direct sulfinylation of 2-halobenzothiazoles and 2-halobenzimidazoles using 尾-sulfinyl esters as the source of the sulfenate ion in the presence of a Bronsted base such as LiOtBu, and the corresponding heteroaryl sulfoxides were isolated in yields of 30 to 94% have been described. Moreover, a plausible concerted nucleophilic aromatic substitution (cSNAr) pathway for the direct incorporation of sulfinyl functionality into the 2-haloheteroarenes has been hypothesized. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3Quality Control of 2-Chlorobenzothiazole).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles are a class of five-membered rings containing nitrogen and sulfur with excellent antitumor, antiviral and antibiotic activities. Electrophilic attack at nitrogen depends on the presence of electron density at nitrogen as well as the position and nature of substituent linked to the thiazole ring.Quality Control of 2-Chlorobenzothiazole

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Luconi, Lapo et al. published their research in Inorganica Chimica Acta in 2021 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles are a class of five-membered rings containing nitrogen and sulfur with excellent antitumor, antiviral and antibiotic activities. The pyridine-type nitrogen in the thiazole ring deactivates the ring for electrophilic substitution reactions, which is further reduced in acid due to protonation of the thiazole ring.Name: 2-Chlorobenzothiazole

Unsymmetrical nickel (PCN) pincer complexes with a benzothiazole side-arm: Synthesis, characterization and electrochemical properties was written by Luconi, Lapo;Tuci, Giulia;Gafurov, Zufar N.;Mercuri, Giorgio;Kagilev, Alexey A.;Pettinari, Claudio;Morozov, Vladimir I.;Yakhvarov, Dmitry G.;Rossin, Andrea;Giambastiani, Giuliano. And the article was included in Inorganica Chimica Acta in 2021.Name: 2-Chlorobenzothiazole This article mentions the following:

The newly prepared unsym. PCN-pincer ligand with a benzothiazole side-arm 2-(3-((di-tert-butylphosphino)methyl)phenoxy)benzothiazole [BzTz(H)PCN] has been cyclometalated with anhydrous NiBr2 to get the corresponding NiII square planar bromo complex [(BzTzPCN)NiBr] (1) after HBr elimination and C-H activation on the pincer central Ph ring. Starting from 1, reaction with AgF in toluene or with AgBF4 in THF led to bromide abstraction and formation of the fluoro complex [(BzTzPCN)NiF] (2) and the ionic aqua species [(BzTzPCN)Ni(H2O)][BF4] (3), resp. All species have been characterized in solution (multinuclear 1H, 13C{1H}, 31P{1H} and 11B NMR spectroscopy) and in the solid state (single-crystal X-ray diffraction anal.). Finally, comparative electrochem. measurements (CV and in situ EPR-spectroelectrochem.) carried out on the halide complexes 1 and 2 revealed that the anodic oxidation process leads to the formation of stable NiIII species bearing a coordinated bromide ligand in case of 1 and a fluoride-free complex in case of 2. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3Name: 2-Chlorobenzothiazole).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles are a class of five-membered rings containing nitrogen and sulfur with excellent antitumor, antiviral and antibiotic activities. The pyridine-type nitrogen in the thiazole ring deactivates the ring for electrophilic substitution reactions, which is further reduced in acid due to protonation of the thiazole ring.Name: 2-Chlorobenzothiazole

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Jafari, Behzad et al. published their research in ChemistrySelect in 2019 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. The thiazole ring has been identified as a central feature of numerous natural products, perhaps the most famous example of which is epothilone. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 2-Chlorobenzothiazole

Synthesis of 2-Alkynyl- and 2-Amino-12H-benzothiazolo[2,3-b]quinazolin-12-ones and Their Inhibitory Potential against Monoamine Oxidase A and B was written by Jafari, Behzad;Jalil, Saquib;Zaib, Sumera;Safarov, Sayfidin;Khalikova, Muattar;Khalikov, Djurabay;Ospanov, Meirambek;Yelibayeva, Nazym;Zhumagalieva, Shynar;Abilov, Zharylkasyn A.;Turmukhanova, Mirgul Z.;Kalugin, Sergey N.;Salman, Ghazwan Ali;Ehlers, Peter;Hameed, Abdul;Iqbal, Jamshed;Langer, Peter. And the article was included in ChemistrySelect in 2019.Recommanded Product: 2-Chlorobenzothiazole This article mentions the following:

The 2-alkynyl- and 2-aminobenzothiazolo[2,3-b]quinazolin-12-ones I (R = isopropylaminyl, diphenylaminyl, morpholin-4-yl, etc.) and II (Ar = Ph, 4-tert-butylphenyl, naphthalen-1-yl, etc.) have been synthesized by Palladium catalyzed Buchwald-Hartwig and Sonogashira reactions. Synthesized derivatives were further evaluated for their role as potential inhibitors of monoamine oxidase A and B (MAO-A and B) isoenzymes. Most compounds possess moderate to excellent inhibitory potential against MAO-A and MAO-B. The 2-amino-substituted derivatives show a significantly higher activity as compared to 2-alkynyl- and previously reported 2-aryl derivatives Studied compounds might be employed as novel monoamine oxidase inhibitors and may provide insights for the development of new drug candidates against neurol. diseases. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3Recommanded Product: 2-Chlorobenzothiazole).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. The thiazole ring has been identified as a central feature of numerous natural products, perhaps the most famous example of which is epothilone. Various laboratory methods exist for the organic synthesis of thiazoles. Prominent is the Hantzsch thiazole synthesis is a reaction between haloketones and thioamides.Recommanded Product: 2-Chlorobenzothiazole

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Kunkle, Trent et al. published their research in Journal of Medicinal Chemistry in 2018 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. There are numerous natural products that possess a thiazole ring with broad pharmacological activities. Thiamine, also known as vitamin B1, possesses a thiazole ring linked with 2-methylpyrimidine-4-amine as hydrochloride salt.Computed Properties of C7H4ClNS

Hydroxybiphenylamide GroEL/ES inhibitors are potent antibacterials against planktonic and biofilm forms of Staphylococcus aureus was written by Kunkle, Trent;Abdeen, Sanofar;Salim, Nilshad;Ray, Anne-Marie;Stevens, Mckayla;Ambrose, Andrew J.;Victorino, Jose;Park, Yangshin;Hoang, Quyen Q.;Chapman, Eli;Johnson, Steven M.. And the article was included in Journal of Medicinal Chemistry in 2018.Computed Properties of C7H4ClNS This article mentions the following:

We recently reported the identification of a GroEL/ES inhibitor (1, N-(4-(benzo[d]thiazol-2-ylthio)-3-chlorophenyl)-3,5-dibromo-2-hydroxybenzamide) that exhibited in vitro antibacterial effects against Staphylococcus aureus comparable to vancomycin, an antibiotic of last resort. To follow up, we have synthesized 43 compound 1 analogs to determine the most effective functional groups of the scaffold for inhibiting GroEL/ES and killing bacteria. Our results identified that the benzothiazole and hydroxyl groups are important for inhibiting GroEL/ES-mediated folding functions, with the hydroxyl essential for antibacterial effects. Several analogs exhibited >50-fold selectivity indexes between antibacterial efficacy and cytotoxicity to human liver and kidney cells in cell culture. We found that MRSA was not able to easily generate acute resistance to lead inhibitors in a gain-of-resistance assay and that lead inhibitors were able to permeate through established S. aureus biofilms and maintain their bactericidal effects. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3Computed Properties of C7H4ClNS).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. Thiazoles in peptides or their ability to bind proteins, DNA and RNA has led to many synthetic studies and new applications. There are numerous natural products that possess a thiazole ring with broad pharmacological activities. Thiamine, also known as vitamin B1, possesses a thiazole ring linked with 2-methylpyrimidine-4-amine as hydrochloride salt.Computed Properties of C7H4ClNS

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Chen, Yuqian et al. published their research in Journal of Solid State Chemistry in 2021 | CAS: 615-20-3

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. The thiazole ring is notable as a component of the vitamin thiamine (B1). Electrophilic attack at nitrogen depends on the presence of electron density at nitrogen as well as the position and nature of substituent linked to the thiazole ring.HPLC of Formula: 615-20-3

One-dimensional La(III) coordination polymer displaying multi-responsive luminescence activities towards Fe3+, acetone and benzothiozoles was written by Chen, Yuqian;Xian, Guoxuan;Yan, Hui;Wang, Yuhao;Li, Yunwu;Lu, Jing;Xu, Haijun;Tao, Jiayu;Wang, Suna. And the article was included in Journal of Solid State Chemistry in 2021.HPLC of Formula: 615-20-3 This article mentions the following:

Through reaction of La(NO3)3 with a flexible carboxylic acid ligand named 3,5-bis[(2-carboxyphenyl)oxy]benzoic acid (H3L) under solvothermal condition, the complex with the formula of [La(L)(DMF)2] (1) was obtained. One-dimensional chain of the complex was generated through the connection of binuclear units of La2(COO)4 across the flexible acid ligands. Luminescence results showed that different pollutants (Fe3+, acetone and benzothiophene organic compounds) could quench the luminescence of the blue emission of the complex in DMF with much low detection limit. Among several 2-substituted benzothiophene compounds, 2,2′-dithiobisbenzothiazole (DM) has a strongest binding constant of 10.8 x 104 M-1 and lowest detection limit of 0.332 μM (0.110 ppm). All quenching effect was found within 15 s. The sensing mechanism was investigated through a series of experiments and theor. calculation Complex 1 could be employed as a multi-responsive chemosensor for detection of different pollutants with high sensitivity and fast response. In the experiment, the researchers used many compounds, for example, 2-Chlorobenzothiazole (cas: 615-20-3HPLC of Formula: 615-20-3).

2-Chlorobenzothiazole (cas: 615-20-3) belongs to thiazole derivatives. The thiazole ring is notable as a component of the vitamin thiamine (B1). Electrophilic attack at nitrogen depends on the presence of electron density at nitrogen as well as the position and nature of substituent linked to the thiazole ring.HPLC of Formula: 615-20-3

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica