Category: 101078-51-7

Synthetic Route of 101078-51-7, 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.101078-51-7, Name is 6-Methoxy-2-(p-tolyl)benzo[d]thiazole, molecular formula is C15H13NOS. In a patent, introducing its new discovery.

2-Aryl benzothiazole formation from aryl ketones and 2-aminobenzenethiols under metal- and I2-free conditions was described. Various 2-aryl benzothiazoles were selectively obtained in good yields using molecular oxygen as oxidant. DMSO played an important role in this transformation. Functional groups such as methyl, methoxy, fluoro, chloro, bromo and nitro groups were tolerated under the optimized reaction conditions.

If you are interested in 101078-51-7, you can contact me at any time and look forward to more communication.Synthetic Route of 101078-51-7

Reference：
Thiazole | C3H7126NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 101078-51-7, Name is 6-Methoxy-2-(p-tolyl)benzo[d]thiazole,molecular formula is C15H13NOS, is a conventional compound. this article was the specific content is as follows.category: thiazole

The reaction of 6-substituted-1,2,3-benzodithiazole-2-oxides (2) with aromatic aldehydes, carboxylic acids and acid chlorides in the presence of an organic base such as triethylamine and N,N-dimethylaniline lead to the formation of 6-substituted-2-arylbenzothiazoles (3).The reaction of 2 with phenacyl bromides and ethyl chloroacetate under similar conditions give 3-aryl-7-substituted-1,4-benzothiazines (4) and 7-substituted-3-oxo-3,4-dihydro-1,4-benzothiazines (5), respectively.This provides a new method for the synthesis of benzothiazoles and 1,4-benzothiazines without involving the preparation of intermediate 2-aminobenzenethiols.

Do you like my blog? If you like, you can also browse other articles about this kind. category: thiazole. Thanks for taking the time to read the blog about 101078-51-7

Reference：
Thiazole | C3H7114NS – 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. 101078-51-7, Name is 6-Methoxy-2-(p-tolyl)benzo[d]thiazole, molecular formula is C15H13NOS. In a Article，once mentioned of 101078-51-7, Safety of 6-Methoxy-2-(p-tolyl)benzo[d]thiazole

An efficient and practical method for the construction of 2-aryl-and 2-alkyl-substituted benzothiazoles via a copper-catalyzed redox condensation process between benzothiazoles and aldehydes or benzylic alcohols has been developed. The reaction proceeded under mild reaction conditions using environmentally benign tert-butyl hydroperoxide (TBHP) as the oxidant. A reaction mechanism involving the ring-opening of benzothiazoles initiated by the attack of acyl radical on the thiazole ring and intramolecular condensation is proposed based on the isolation of an anilide disulfide intermediate.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of 6-Methoxy-2-(p-tolyl)benzo[d]thiazole. In my other articles, you can also check out more blogs about 101078-51-7

Reference：
Thiazole | C3H7117NS – 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. 101078-51-7, Name is 6-Methoxy-2-(p-tolyl)benzo[d]thiazole, molecular formula is C15H13NOS. In a Article£¬once mentioned of 101078-51-7, name: 6-Methoxy-2-(p-tolyl)benzo[d]thiazole

A highly efficient method for the synthesis of 2-arylbenzothiazoles has been developed using readily available aromatic amines, benzaldehydes, and NH4SCN as a sulfur source. A library of 2-arylbenzothiazoles with wide functional group compatibility has been synthesized in good yields through iodine-mediated oxidative annulation.

A highly efficient method for the synthesis of 2-arylbenzothiazoles has been developed using readily available aromatic amines, benzaldehydes, and NH4SCN as a sulfur source. A library of 2-arylbenzothiazoles with wide functional group compatibility has been synthesized in good yields through iodine-mediated oxidative annulation.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: 6-Methoxy-2-(p-tolyl)benzo[d]thiazole. In my other articles, you can also check out more blogs about 101078-51-7

Reference£º
Thiazole | C3H7124NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 101078-51-7, Name is 6-Methoxy-2-(p-tolyl)benzo[d]thiazole,molecular formula is C15H13NOS, is a conventional compound. this article was the specific content is as follows.Recommanded Product: 101078-51-7

Nontransition metal-catalyzed synthesis of 2-aryl benzothiazoles was achieved through K2S2O8-mediated oxidative condensation of benzothiazoles with aryl aldehydes. The same transformation can also be effected when the aryl aldehydes were replaced with phenylglyoxylic acids.

Nontransition metal-catalyzed synthesis of 2-aryl benzothiazoles was achieved through K2S2O8-mediated oxidative condensation of benzothiazoles with aryl aldehydes. The same transformation can also be effected when the aryl aldehydes were replaced with phenylglyoxylic acids.

Do you like my blog? If you like, you can also browse other articles about this kind. Recommanded Product: 101078-51-7. Thanks for taking the time to read the blog about 101078-51-7

Reference£º
Thiazole | C3H7115NS – 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.101078-51-7, Name is 6-Methoxy-2-(p-tolyl)benzo[d]thiazole, molecular formula is C15H13NOS. In a Article£¬once mentioned of 101078-51-7, COA of Formula: C15H13NOS

2-Substituted benzothiazoles were efficiently synthesized by radical cyclization of thioformanilides induced by chloranil under irradiation in 1,2-dichloroethane and toluene at 80 C. Hydrogen atom abstraction from thiobenzamide by triplet chloranil was the key step of the mechanism, as confirmed by LFP experiments. The methodology developed is simple and afforded the easily isolated products from moderate to good yield.

2-Substituted benzothiazoles were efficiently synthesized by radical cyclization of thioformanilides induced by chloranil under irradiation in 1,2-dichloroethane and toluene at 80 C. Hydrogen atom abstraction from thiobenzamide by triplet chloranil was the key step of the mechanism, as confirmed by LFP experiments. The methodology developed is simple and afforded the easily isolated products from moderate to good yield.

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.COA of Formula: C15H13NOS, you can also check out more blogs about101078-51-7

Reference£º
Thiazole | C3H7125NS – PubChem,
Thiazole | chemical compound | Britannica