Category: 73458-39-6

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.73458-39-6, Name is 5-Nitrobenzo[d]thiazol-2-amine, molecular formula is C7H5N3O2S. In a Article，once mentioned of 73458-39-6, Formula: C7H5N3O2S

A series of substituted 2-aminobenzothiazole compounds have been synthesized and evaluated as nitric oxide synthase (NOS) inhibitors. Compound 14 shows activity in the nM range and is selective for the human neuronal NOS isoform. We have also evaluated the compounds against the rat NOS isoforms. For some of the compounds, there are significant differences in NOS inhibitory activities between the human and rat enzymes. For example, compound 10b has nM activity against the rat nNOS while low muM activity against the human nNOS.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 73458-39-6 is helpful to your research., Formula: C7H5N3O2S

Reference：
Thiazole | C3H6563NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products of 73458-39-6, An article , which mentions 73458-39-6, molecular formula is C7H5N3O2S. The compound – 5-Nitrobenzo[d]thiazol-2-amine played an important role in people’s production and life.

Reaction between substituted thiazolylamine or oxazolylamine, triethyl orthoformate and sodium azide in the presence of tributylmethylammonium chloride in DMSO furnishes 1-substituted 1H-1,2,3,4-tetrazole in high yield.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 73458-39-6, help many people in the next few years., Related Products of 73458-39-6

Reference：
Thiazole | C3H6550NS – PubChem,
Thiazole | chemical compound | Britannica

Reference of 73458-39-6, Chemistry can be defined as the study of matter and the changes it undergoes. You’ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.73458-39-6, Name is 5-Nitrobenzo[d]thiazol-2-amine, molecular formula is C7H5N3O2S. In a patent, introducing its new discovery.

New dichromophoric cyanine dyes based on benzothiazol-2-amines as push-pull systems were synthesized in two series of disperse and cationic forms (see 4 in Scheme1 and 5 in Scheme2, resp.). Their thermal stabilities, UV/VIS, fluorescence, and solvatochromic behavior, which are important parameters in push-pull systems, were also studied.

If you are interested in 73458-39-6, you can contact me at any time and look forward to more communication.Related Products of 73458-39-6

Reference：
Thiazole | C3H6552NS – PubChem,
Thiazole | chemical compound | Britannica

73458-39-6, Name is 5-Nitrobenzo[d]thiazol-2-amine, molecular formula is C7H5N3O2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 73458-39-6, Recommanded Product: 73458-39-6

The kinetics of methoxide ion-catalysed solvolysis of 1-acyl-3-(2-halo-5-nitrophenyl)thioureas and cyclization of fluoro derivatives were studied in methanol at 25 deg C. The cyclization involved the substitution of fluorine by sulphur anion of thiourea and proceeded in two steps. With the acetyl derivative, the first step is methanolysis and the second step is much slower cyclization of the 2-fluoro-5-nitrophenylthiourea anion formed to give 2-amino-5-nitro-1,3-benzothiazole. With the benzoyl derivative, the first step involves parallel methanolysis of the benzoyl group and cyclization to 2-benzoylamino-5-nitro-1,3-benzothiazole. At concentrations of sodium methoxide higher than ca. 0.01 mol l-1 the rates of solvolyses of all the acyl halothioureas decreased and at concentrations higher than ca. 0.01 mol l-1 the rates of solvolyses of all the acyl halothioureas decreased and at concentrations higher than ca. 0.4 mol l-1 there was an increase in the formation of other product(s) than the product of cyclization. After the addition of 18-crown-6, the side products were not formed and the cyclization of fluoro derivatives were considerably accelerated. The slowing of the solvolytic reaction and acceleration of the cyclization reaction are most probably due to the formation of dianions.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 73458-39-6. In my other articles, you can also check out more blogs about 73458-39-6

Reference：
Thiazole | C3H6545NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products of 73458-39-6. Let’s face it, organic chemistry can seem difficult to learn. Especially from a beginner’s point of view. Like 73458-39-6, Name is 5-Nitrobenzo[d]thiazol-2-amine. In a document type is Article, introducing its new discovery.

The polarographic reduction of 5-(2′-benzothiazolylhydrazono)-1,3-dimethylbarbituric acids takes place in a single four-electron transfer step, giving diffusion-controlled irreversible waves in BR buffers in the pH range 2.2 to 10.6.The effect of substituents, various cations and solvent composition on the electrode reaction is discussed.

If you are interested in 73458-39-6, you can contact me at any time and look forward to more communication.Related Products of 73458-39-6

Reference：
Thiazole | C3H6544NS – PubChem,
Thiazole | chemical compound | Britannica

73458-39-6, Name is 5-Nitrobenzo[d]thiazol-2-amine, molecular formula is C7H5N3O2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 73458-39-6, Application In Synthesis of 5-Nitrobenzo[d]thiazol-2-amine

The title compounds (5a-j), (6a-j), and (7a-j) were prepared via a four-step procedure using starting material 4-methoxyaniline (1). The structure of all synthesized compounds was confirmed by FT-IR, 1H NMR, 13C NMR, and CHN analysis. The synthesized compounds were tested for their antibacterial and antifungal activity (MIC) in vitro against organisms viz. B. subtilis, S. aureus, E. coli, P. aeruginosa, and C. albicans taking ciprofloxacin, ampicillin, streptomycin, penicillin-G, fluconazole, and nystatin as the standard drugs. Some of the compounds have shown significant activities.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of 5-Nitrobenzo[d]thiazol-2-amine. In my other articles, you can also check out more blogs about 73458-39-6

Reference：
Thiazole | C3H6536NS – PubChem,
Thiazole | chemical compound | Britannica

73458-39-6, Name is 5-Nitrobenzo[d]thiazol-2-amine, molecular formula is C7H5N3O2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 73458-39-6, Recommanded Product: 5-Nitrobenzo[d]thiazol-2-amine

Based on 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid[2- (cyclohexanecarbonylamino)benzothiazol-6-yl]amide (1), which shows selective cytotoxicity against tumorigenic cell lines, 2,6-dichloro-N-[2- (cyclopropanecarbonylamino)benzothiazol-6-yl]benzamide (13b) was designed and synthesized as a biologically stable derivative containing no nitro group. The highly potent derivative 13b exhibited excellent in vivo inhibitory effect on tumor growth.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 5-Nitrobenzo[d]thiazol-2-amine. In my other articles, you can also check out more blogs about 73458-39-6

Reference：
Thiazole | C3H6561NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.73458-39-6, Name is 5-Nitrobenzo[d]thiazol-2-amine, molecular formula is C7H5N3O2S. In a Article，once mentioned of 73458-39-6, Product Details of 73458-39-6

The synthesis and evaluation of antiplasmodial activity of benzothiazole, benzimidazole, benzoxazole and pyridine analogues of amodiaquine is hereby reported. Benzothiazole and benzoxazole analogues with a protonatable tertiary nitrogen atom possessed excellent activity against the W2 and K1 chloroquine resistant strains of Plasmodium falciparum, with IC50s ranging from 7 to 22 nM.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 73458-39-6, you can also check out more blogs about73458-39-6

Reference：
Thiazole | C3H6538NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.73458-39-6, Name is 5-Nitrobenzo[d]thiazol-2-amine, molecular formula is C7H5N3O2S. In a Article，once mentioned of 73458-39-6, Safety of 5-Nitrobenzo[d]thiazol-2-amine

Synthesis and antibacterial activity of a novel series of 2,3-diaryl-substituted-imidazo(2,1-b)-benzothiazole derivatives

Benzothiazole and imidazole compounds are extensively studied heterocyclics due to their wide spectrum of bioactivities. Among them, the imidazo(2,1-b)-benzothiazole derivatives are pharmacologically important because of their immunostimulant, anti-inflammatory, antifungal, antimicrobial, antitumor, and other activities. In the present research work, a novel series of 2,3-diaryl-substituted imidazo(2,1-b)-benzothiazoles 13a-o have been synthesized by reaction of substituted 2-aminobenzothiazoles 1-8 and an appropriately substituted a-bromo-1-(4?-substituted)-phenyl-2-(4?- substituted)-phenyl-1-ethanones 9-12 in the presence of anhydrous acetonitrile. They were characterized by physicochemical, elemental, and spectral (IR, 1H-NMR, and Mass) data. All the synthesized compounds were screened for their in-vitro antibacterial activity against Gram-positive, Gram-negative bacteria. The investigation of antibacterial screening data revealed that most of the compounds tested have demonstrated congruent activity against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa as compared with the standard ampicillin. Among the series, compounds 13d, 13h, and 13m exhibited excellent an antibacterial activity profile as compared with the standard. In summary, preliminary results indicate that some of the newly synthesized title compounds exhibited promising antibacterial activities and they warrant more consideration as prospective antimicrobials.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 73458-39-6 is helpful to your research., Safety of 5-Nitrobenzo[d]thiazol-2-amine

Reference：
Thiazole | C3H6560NS – PubChem,
Thiazole | chemical compound | Britannica