Category: 16112-21-3

Electric Literature of 16112-21-3, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS. In a Article，once mentioned of 16112-21-3

Synthesis of 2-Arylbenzothiazole and 2-Arylthiazole Derivatives via a Ru-Catalyzed meta-Selective C-H Nitration Reaction

A Ru-catalyzed meta-selective C-H nitration of 2-arylbenzothiazoles and 2-arylthiazoles has been developed. A wide range of functional groups are tolerated, providing the meta-nitrated products in good to excellent yields using Cu(NO3)2·3H2O as the nitro source. The nitration could be carried out on a gram scale and used for the synthesis of promising therapeutic leads for human African trypanosomiasis.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 16112-21-3 is helpful to your research., Electric Literature of 16112-21-3

Reference：
Thiazole | C3H828NS – PubChem,
Thiazole | chemical compound | Britannica

16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 16112-21-3, Computed Properties of C14H11NS

Syntheses of 2-aryl benzothiazoles via photocatalyzed oxidative condensation of amines with 2-aminothiophenol in the presence of bodipy derivatives

A simple, convenient, and efficient new method for synthesis of 2-aryl benzothiazoles under mild conditions with nonmetal catalyst has been developed. Boron-dipyrromethene (BODIPY) dyes were used as photocatalysts for aerobic oxidative reactions of amine with 2-aminothiophenol. The approach will be very useful for the synthesis of benzothiazole derivatives and the development of photocatalytic reactions.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Computed Properties of C14H11NS. In my other articles, you can also check out more blogs about 16112-21-3

Reference：
Thiazole | C3H809NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products of 16112-21-3, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 16112-21-3, C14H11NS. A document type is Patent, introducing its new discovery.

A medicine intermediate 2 – aryl benzo thiazole synthetic method of compound (by machine translation)

The invention relates to a kind of the following formula (III) is shown in the 2 – aryl benzo thiazole compound synthesis method, The method includes: in the three-component composite in the solvent, the catalyst, in the presence of alkali and accelerator, the following formula (I) compound with the following formula (II) compound to react, thus get the states the type (III) compound, Wherein R1 , R2 Are each independently selected from H, C1 – C6 Alkyl, C1 – C6 Alkoxy, halogen or nitro; X is halogen. The method through the catalyst, alkali, accelerator and three-component solvent system selected, combined, so as to play a unique synergy, achieved excellent product yield, has industrial application in the medical field of the actual value. (by machine translation)

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Reference：
Thiazole | C3H644NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 16112-21-3, An article , which mentions 16112-21-3, molecular formula is C14H11NS. The compound – 2-(4-Methylphenyl)benzothiazole played an important role in people’s production and life.

Iron-catalyzed arylation of benzoazoles with aromatic aldehydes using oxygen as oxidant

An iron-catalyzed arylation of azoles with aromatic aldehydes using oxygen as oxidant has been discovered. The reaction proceeded well for a range of different substrates under oxidative conditions. The Royal Society of Chemistry.

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Reference：
Thiazole | C3H762NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS. In a Article，once mentioned of 16112-21-3, Formula: C14H11NS

FeCl3/ultrasound mediated reaction of 2-aminothiophenol with aldehydes in water: Synthesis of 2-substituted benzothiazoles of pharmacological interest

We report a FeCl3?6H2O mediated green and rapid access to benzothiazole derivatives having a substituent at C-2 via the condensation of 2-aminothiophenol with various aldehydes under ultrasound irradiation and air. The reaction progressed well in water affording the expected products in good yields. Two of these compounds known to be potent anticancer agents showed good interactions with PDE4B in silico and inhibited this enzyme when tested in vitro.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Formula: C14H11NS. In my other articles, you can also check out more blogs about 16112-21-3

Reference：
Thiazole | C3H603NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 16112-21-3, An article , which mentions 16112-21-3, molecular formula is C14H11NS. The compound – 2-(4-Methylphenyl)benzothiazole played an important role in people’s production and life.

Copper-Catalyzed Chelation-Assisted ortho-Nitration of 2-Aryls Using Pharmacophoric Benzothiazoles and Benzoxazoles as Directing Groups

A copper-catalyzed chelation-assisted ortho-nitration reaction of aryl derivtives has been achieved, using benzazoles as efficient directing groups. The reaction is general and efficient for aryl derivatives with various electronic properties, and also with different pharmacophorically important directing groups, i.e., benzoxazoles, benzothiazoles, and benzimidazoles. The nitro-group-containing products have significance as fluorogenic compounds and potential nitroreductase substrates that could be used for the detection of clinically important microorganisms. The nitration reaction proceeds with an inexpensive copper catalyst and a mild, cheap, and environmentally friendly nitro source, Fe(NO3)3·9H2O. This operationally simple and functional-group-tolerant protocol for the nitration of 2-aryl benzazoles proceeds with a high regioselectivity without the exclusion of air or moisture.

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Reference：
Thiazole | C3H888NS – PubChem,
Thiazole | chemical compound | Britannica

16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 16112-21-3, Formula: C14H11NS

Graphene oxide as a heterogeneous reagent promoted synthesis of 2-substituted 1,3-benzazoles in water

An efficient chemical method for the synthesis of benzimidazoles, benzothiazoles, and benzoxazoles has been developed through the condensation of various aldehydes with o-phenylenediamine, o-aminothiophenol, and o-aminophenol using graphene oxide (GO) as an oxidant in water. These benzazoles are also prepared through a one-pot oxidation/condensation tandem process by reacting alcohols with 2-amino-(thio)phenol/aniline in the presence of GO in poly(ethylene glycol) as a safe media. Moreover, this carbonaceous material could be readily separated using a simple filtration.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Formula: C14H11NS. In my other articles, you can also check out more blogs about 16112-21-3

Reference：
Thiazole | C3H778NS – PubChem,
Thiazole | chemical compound | Britannica

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 16112-21-3, C14H11NS. A document type is Article, introducing its new discovery., name: 2-(4-Methylphenyl)benzothiazole

Sulfonic-acid-functionalized activated carbon made from tea leaves as green catalyst for synthesis of 2-substituted benzimidazole and benzothiazole

Abstract: A simple and efficient procedure for synthesis of 2-substituted benzimidazole and benzothiazole has been developed by using sulfonic-acid-functionalized activated carbon as heterogeneous catalyst. The activated material was prepared from matured tea leaf in presence of phosphoric acid as activating agent. The final catalyst was prepared by anchoring ?SO3H group on the surface of the activated carbon. The catalyst could be easily recovered and reused for more than three catalytic cycles without significant loss in catalytic activity. The catalytic performance of the catalyst was found to be superior to that of a similar catalyst prepared from montmorillonite K10. Graphical Abstract: [Figure not available: see fulltext.].

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Reference：
Thiazole | C3H796NS – PubChem,
Thiazole | chemical compound | Britannica

16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 16112-21-3, SDS of cas: 16112-21-3

Iron-catalyzed direct C-H arylation of heterocycles and quinones with arylboronic acids

The arylation of C-H bonds to generate heteroaryl-aryl (Het-Ar) and arylated quinone (Quin-Ar) compounds has received great attention to achieve sustainable goals in synthetic chemistry. Despite significant advances, arylation of a broad range of Het-Ar and Quin-Ar derivatives remains a challenging task. Herein, a variety of heterocycles are arylated by using arylboronic acids in the presence of catalytic amounts of inexpensive Fe(NO 3)3. The C-arylated quinone compounds can be prepared by reacting arylboronic acids with either quinone or hydroquinone. The present method is operationally simple, scalable, does not require prefunctionalization of the heterocycle or quinone, and can tolerate a wide variety of functional groups in the coupling partners. These qualities are expected to render this method attractive for academic and industrial use. Direct C-H arylation of a variety of heterocycles and quinones with arylboronic acids has been developed. An inexpensive iron catalyst, Fe(NO3)3, and a co-oxidant, persulfate, were used in air. The protocol is applicable for large-scale synthesis and is expected to find application as a result of its operational simplicity. Copyright

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.SDS of cas: 16112-21-3. In my other articles, you can also check out more blogs about 16112-21-3

Reference：
Thiazole | C3H666NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 16112-21-3, 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.16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS. In a patent, introducing its new discovery.

Reactions of Carboxylic Acids with “Phosphonium Anhydrides”

General considerations are outlined for a reagent to extract oxygen from organic molecules by an equivalent of dehydration.Reagents, (R3P+)2O, 2OTf-, were created for the purpose and subjected to a preliminary study.They were found to convert carboxylic acids readily and rapidly to anhydrides, esters, amides, amidines, benzimidazoles, and cyclic aryl ketones in good yields.

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Reference：
Thiazole | C3H727NS – PubChem,
Thiazole | chemical compound | Britannica