Category: 16112-21-3

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

The cyclocondensation of 2-aminothiophenol and aldehydes has been carried out in dichloromethane using bakers’ yeast as a catalyst for obtaining 2-aryl/heteryl benzothiazoles in good yields.

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 | C3H660NS – 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.16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS. In a Article，once mentioned of 16112-21-3, Application In Synthesis of 2-(4-Methylphenyl)benzothiazole

(-)-cis-2,3-Dihydro-3-(4-methylpiperazinylmethyl)-2-phenyl-1,5-benzothiazepin-4(5H)-one hydrochloride (BTM-1086) and its analogues, which possessed potent anti-ulcer and gastric secretory inhibiting activities, were synthesized and the structure of these compounds were established on the basis of spectral and chemical evidences.

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.HPLC of Formula: C14H11NS, you can also check out more blogs about16112-21-3

Reference：
Thiazole | C3H916NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route 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

2,4,6-Trichloro-1,3,5-triazine efficiently catalyzed the condensation reactions between 2-aminothiophenol and aromatic aldehydes to afford 2-arylbenzothiazolles in good-to-excellent yields. Simple and mild reaction conditions, the use of a cheap catalyst and easy work up, and isolation are notable features of this method.

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., Synthetic Route of 16112-21-3

Reference：
Thiazole | C3H911NS – 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, Computed Properties of C14H11NS

A series of 4-(benzothiazol-2-yl)benzylphosphonic acid dialkyl ester were synthesized and evaluated for coronary vasodilatory activity by Langendorff’s method in the isolated guinea pig heart. Many of the phosphonic acid dialkyl esters exhibited vasodilatory activity and calcium antagonism comparable with those of diltiazem hydrochloride, whereas phosphonic acid 1b and its nonphosphonated precursor 7a were inactive.These results indicate the necessity of the diethoxyphosphinyl moiety for vasodilatory activity.Substitution of the benzothiazole ring with a variety of substituents did not significantly enhance the activity of the unsubstituted compound.Compound 10b (KB-944) was chosen for detailed pharmacological evaluation.

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 | C3H822NS – 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, SDS of cas: 16112-21-3

Simple and eco-friendly synthesis of 2-substituted benzothiazoles is described. The reaction is performed in absolute ethanol at room temperature, using a catalytic amount of montmorillonite K-10, and with continuous bubbling of air as oxidant. Simplicity, ease of handling of the system, an environmentally friendly and reusable catalyst, a plentiful, inexpensive, and safe oxidant, and mild conditions are the main advantages of this procedure.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.SDS of cas: 16112-21-3, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 16112-21-3, in my other articles.

Reference：
Thiazole | C3H676NS – 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, HPLC of Formula: C14H11NS

One-pot condensation of 2-aminothiophenol or 1,2-phenylenediamine with different aldehydes has been catalyzed by hexamethylenetetramine-bromine (HMTA-Bromine) as new, available and effective catalyst. 2-Arylbenzo-thiazoles and 2-aryl-benzimidazoles have been achieved in excellent yield and good purity.

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

Reference：
Thiazole | C3H689NS – 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, Recommanded Product: 2-(4-Methylphenyl)benzothiazole

A cheap and recyclable ZnO-beta zeolite was used as catalyst for the synthesis of benzothiazole derivatives. This method provides several advantages such as environmental friendliness, short reaction times, high yields, simple work-up procedure and catalyst was successfully reused for four cycles without significant loss of activity.

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

Reference：
Thiazole | C3H895NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products 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.

A series of amido pincer complexes of nickel were examined for their catalysis in the Kumada cross-coupling reaction. The P,N,O-pincer nickel complexes tested are active catalysts for the cross-coupling of aryl, heteroaryl, and vinyl chlorides with aryl Grignard reagents. The reactions can proceed at room temperature and tolerate functional groups in aryl chlorides with the aid of LiCl and ZnCl2 additives (Figure presented).

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Reference：
Thiazole | C3H821NS – 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., Quality Control of: 2-(4-Methylphenyl)benzothiazole

CuO nanospindles have been developed to efficiently catalyze the direct arylation of heterocycle C-H bonds with moderate to excellent yields. This reaction can be applied to heterocycles such as benzoxazole, benzothiazole, and 1-methylbenzimidazole in the presence of a more environmentally friendly inorganic base like K2CO3 under ligand-free catalytic conditions. In addition, the catalyst can be recycled and reused without any significant decrease in catalytic activity.

Interested yet? Keep reading other articles of 16112-21-3!, Quality Control of: 2-(4-Methylphenyl)benzothiazole

Reference：
Thiazole | C3H739NS – 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

Benzothiazole derivatives are prepared via reductive cyclization of nitrodisulfides with nitriles promoted by SmI2 under mild and neutral conditions.

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 | C3H749NS – PubChem,
Thiazole | chemical compound | Britannica