Category: 51618-29-2

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.51618-29-2, Name is 6-Chlorobenzo[d]thiazole-2-thiol, molecular formula is C7H4ClNS2. In a Article，once mentioned of 51618-29-2, SDS of cas: 51618-29-2

Screening and characterization of an inhibitory chemical specific to Arabidopsis gibberellin 2-oxidases

The hydroxylation of gibberellin (GA) at the 2-position is known as the major cause of inactivation of GAs, whose reaction is catalyzed by 2-oxoglutarate dependent dioxygenases, also termed GA 2-oxidases (GA2oxs). To block GA catabolism in plants, a few chemicals can be used. To obtain novel inhibitors specific to GA2oxs, we performed in vitro random screenings by using 3H-16,17-dihydro-GA4 and recombinant Arabidopsis GA2ox2. As a result, one candidate, methyl 6-chloro-3H-1,2,3-benzodithiazole-4-carboxylate 2-oxide (CBTC), was selected from the screening, and was subjected to in-planta evaluations. CBTC promoted both the germination and elongation of Arabidopsis seedlings. This strongly suggests that CBTC inhibits GA2oxs in Arabidopsis with high specificity.

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.SDS of cas: 51618-29-2, you can also check out more blogs about51618-29-2

Reference：
Thiazole | C3H6992NS – 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. 51618-29-2, Name is 6-Chlorobenzo[d]thiazole-2-thiol, molecular formula is C7H4ClNS2. In a Article£¬once mentioned of 51618-29-2, category: thiazole

An unprecedented asymmetric desymmetrization of meso-epoxides, derived from cyclopentene-1,3-diones, with 2-mercaptobenzothiazoles has been realized. It was efficiently catalyzed by a chiral DyIII/N,N?-dioxide complex through a thiolysis/elimination sequence. This remote stereocontrol strategy provides facile access to synthetically versatile cyclopentene derivatives bearing an all-carbon quaternary stereogenic center in high yield and excellent enantioselectivity. Intriguingly, optically active thiophene could be readily generated from the obtained product through an efficient one-pot protocol. Cap it all: The title reaction of meso-diketoepoxides with 2-mercaptobenzothiazoles has been realized. An array of cyclopentene-1,3-diones bearing an all-carbon quaternary stereogenic center were obtained in high yield and excellent enantioselectivity. This methodology paves the way for the construction of optically active thiophenes.

An unprecedented asymmetric desymmetrization of meso-epoxides, derived from cyclopentene-1,3-diones, with 2-mercaptobenzothiazoles has been realized. It was efficiently catalyzed by a chiral DyIII/N,N?-dioxide complex through a thiolysis/elimination sequence. This remote stereocontrol strategy provides facile access to synthetically versatile cyclopentene derivatives bearing an all-carbon quaternary stereogenic center in high yield and excellent enantioselectivity. Intriguingly, optically active thiophene could be readily generated from the obtained product through an efficient one-pot protocol. Cap it all: The title reaction of meso-diketoepoxides with 2-mercaptobenzothiazoles has been realized. An array of cyclopentene-1,3-diones bearing an all-carbon quaternary stereogenic center were obtained in high yield and excellent enantioselectivity. This methodology paves the way for the construction of optically active thiophenes.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.category: thiazole. In my other articles, you can also check out more blogs about 51618-29-2

Reference£º
Thiazole | C3H7008NS – PubChem,
Thiazole | chemical compound | Britannica

51618-29-2, Name is 6-Chlorobenzo[d]thiazole-2-thiol, molecular formula is C7H4ClNS2, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 51618-29-2, Quality Control of: 6-Chlorobenzo[d]thiazole-2-thiol

Novel O- S,O- S,S- N,N- and N,S-substituted naphthoquinone compounds were prepared by reaction of 2,3-dichloro-1,4-naphthoquinone and the corresponding nucleophiles in the presence of chloroform and triethylamine or ethanol solution of Na2CO3. The structures of the novel naphthoquinone compounds were characterized by micro analysis, FT-IR, UV/Vis, 1H NMR, 13C NMR, MS, and fluorescence spectroscopy. Copyright Taylor & Francis Group, LLC.

Novel O- S,O- S,S- N,N- and N,S-substituted naphthoquinone compounds were prepared by reaction of 2,3-dichloro-1,4-naphthoquinone and the corresponding nucleophiles in the presence of chloroform and triethylamine or ethanol solution of Na2CO3. The structures of the novel naphthoquinone compounds were characterized by micro analysis, FT-IR, UV/Vis, 1H NMR, 13C NMR, MS, and fluorescence spectroscopy. Copyright Taylor & Francis Group, LLC.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Quality Control of: 6-Chlorobenzo[d]thiazole-2-thiol. In my other articles, you can also check out more blogs about 51618-29-2

Reference£º
Thiazole | C3H7001NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 51618-29-2, 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.51618-29-2, Name is 6-Chlorobenzo[d]thiazole-2-thiol, molecular formula is C7H4ClNS2. In a patent, introducing its new discovery.

The present invention provides a green synthetic 2 the thiazole derivatives microballoonses […] and method, the method comprises: the neighbouring amidogen aromatic disulfide, CS 2, metal sulfide and solvent, to obtain the 2 […] mercaptobenzothiazole derivatives, the solvent is water, lower alcohol, DMSO, DMF, NMP or 1,4 the dioxane […] in at least one of. Compared with the prior art, the invention utilizes O-amino-aromatic disulfide react with carbon disulfide, the quickly and efficiently the 2 […] mercaptobenzothiazole derivatives, the used raw material is stable and easy to obtain, the cost is low, synthetic method is simple and convenient to operate, the step is short, high yield, the product is easy to be purified. (by machine translation)

The present invention provides a green synthetic 2 the thiazole derivatives microballoonses […] and method, the method comprises: the neighbouring amidogen aromatic disulfide, CS 2, metal sulfide and solvent, to obtain the 2 […] mercaptobenzothiazole derivatives, the solvent is water, lower alcohol, DMSO, DMF, NMP or 1,4 the dioxane […] in at least one of. Compared with the prior art, the invention utilizes O-amino-aromatic disulfide react with carbon disulfide, the quickly and efficiently the 2 […] mercaptobenzothiazole derivatives, the used raw material is stable and easy to obtain, the cost is low, synthetic method is simple and convenient to operate, the step is short, high yield, the product is easy to be purified. (by machine translation)

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Reference£º
Thiazole | C3H6987NS – 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. 51618-29-2, Name is 6-Chlorobenzo[d]thiazole-2-thiol, molecular formula is C7H4ClNS2. In a Patent£¬once mentioned of 51618-29-2, Application In Synthesis of 6-Chlorobenzo[d]thiazole-2-thiol

A process for the manufacture of 2,6-dichlorobenzoxazole and 2,6-dichlorobenzthiazole by chlorinating K+ or Na+ salts of 6-chloro-2-mercaptobenzoxazole or of 6-chloro-2-mercaptobenzthiazole in halogenated hydrocarbons as suspending agents.

A process for the manufacture of 2,6-dichlorobenzoxazole and 2,6-dichlorobenzthiazole by chlorinating K+ or Na+ salts of 6-chloro-2-mercaptobenzoxazole or of 6-chloro-2-mercaptobenzthiazole in halogenated hydrocarbons as suspending agents.

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 6-Chlorobenzo[d]thiazole-2-thiol. In my other articles, you can also check out more blogs about 51618-29-2

Reference£º
Thiazole | C3H7010NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 51618-29-2, Name is 6-Chlorobenzo[d]thiazole-2-thiol,molecular formula is C7H4ClNS2, is a conventional compound. this article was the specific content is as follows.category: thiazole

A series of 2-alkylthio derivatives of hetaryl thiols were synthesized by selective S-alkylation with alkyl halides (bromides and iodides) with ultrasonic irradiation at room temperature. The reaction was found to be generally applicable to hetaryl thiol derivatives with different substituents in the aromatic nucleus and various alkyl halides. The reaction gives high to excellent yields of products with high purity.

A series of 2-alkylthio derivatives of hetaryl thiols were synthesized by selective S-alkylation with alkyl halides (bromides and iodides) with ultrasonic irradiation at room temperature. The reaction was found to be generally applicable to hetaryl thiol derivatives with different substituents in the aromatic nucleus and various alkyl halides. The reaction gives high to excellent yields of products with high purity.

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Reference£º
Thiazole | C3H7009NS – PubChem,
Thiazole | chemical compound | Britannica