Category: 55690-60-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.55690-60-3, Name is 5-Methoxybenzo[d]thiazole-2-thiol, molecular formula is C8H7NOS2. In a Patent£¬once mentioned of 55690-60-3, Computed Properties of C8H7NOS2

A preparation method of benzene saisai fungus ester, (E)- 2 – (2′ – chloromethyl) phenyl – 3 – methoxy-acrylic acid methyl ester (1) and 6 – methoxy – 2 – mercapto-benzothiazole (2) in the organic solvent and the presence of an alkali, in 60 – 140 C lower reaction to obtain the […]. The invention uses (E)- 2 – (2′ – chloromethyl) phenyl – 3 – methoxy methyl acrylate CN101268780B compared with the intermediate (III) low cost, good atom economy, so that the cost is low. Further, the preparation method of this invention the process is relatively simple, in the course of operating the applied reagent and the toxicity is relatively low, and the mild reaction conditions, the reaction time is short, high yield, high purity, three wastes, is suitable for industrial production. (by machine translation)

A preparation method of benzene saisai fungus ester, (E)- 2 – (2′ – chloromethyl) phenyl – 3 – methoxy-acrylic acid methyl ester (1) and 6 – methoxy – 2 – mercapto-benzothiazole (2) in the organic solvent and the presence of an alkali, in 60 – 140 C lower reaction to obtain the […]. The invention uses (E)- 2 – (2′ – chloromethyl) phenyl – 3 – methoxy methyl acrylate CN101268780B compared with the intermediate (III) low cost, good atom economy, so that the cost is low. Further, the preparation method of this invention the process is relatively simple, in the course of operating the applied reagent and the toxicity is relatively low, and the mild reaction conditions, the reaction time is short, high yield, high purity, three wastes, is suitable for industrial production. (by machine translation)

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 55690-60-3 is helpful to your research., Computed Properties of C8H7NOS2

Reference£º
Thiazole | C3H6458NS – 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.55690-60-3, Name is 5-Methoxybenzo[d]thiazole-2-thiol, molecular formula is C8H7NOS2. In a Article£¬once mentioned of 55690-60-3, Product Details of 55690-60-3

A highly efficient kinetic resolution of racemic 2-acyl-3-aryl-N-tosylaziridines is achieved through a chiral Lewis acid promoted ring-opening reaction with 2-mercaptobenzothiazoles as the nucleophiles. The chiral N,N?-dioxide-lanthanum complex as catalyst and the 2-mercaptobenzothiazoles as active sulfur nucleophiles are the keys to the success of the reaction. A variety of enantioenriched beta-amino thioethers and aziridines are obtained in good yields with good ee values.

A highly efficient kinetic resolution of racemic 2-acyl-3-aryl-N-tosylaziridines is achieved through a chiral Lewis acid promoted ring-opening reaction with 2-mercaptobenzothiazoles as the nucleophiles. The chiral N,N?-dioxide-lanthanum complex as catalyst and the 2-mercaptobenzothiazoles as active sulfur nucleophiles are the keys to the success of the reaction. A variety of enantioenriched beta-amino thioethers and aziridines are obtained in good yields with good ee values.

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 55690-60-3, you can also check out more blogs about55690-60-3

Reference£º
Thiazole | C3H6464NS – 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.55690-60-3, Name is 5-Methoxybenzo[d]thiazole-2-thiol, molecular formula is C8H7NOS2. In a Patent, authors is Yamashita, Tohru£¬once mentioned of 55690-60-3, 55690-60-3

The present invention provides to a compound having an ACC inhibitory action, which is useful as an agent for the prophylaxis or treatment of obesity, diabetes, hypertension, hyperlipidemia, cardiac failure, diabetic complications, metabolic syndrome, sarcopenia, cancer and the like, and has superior efficacy. The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification.

The present invention provides to a compound having an ACC inhibitory action, which is useful as an agent for the prophylaxis or treatment of obesity, diabetes, hypertension, hyperlipidemia, cardiac failure, diabetic complications, metabolic syndrome, sarcopenia, cancer and the like, and has superior efficacy. The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification.

The reactant in an enzyme-catalyzed reaction is called a substrate. 55690-60-3 Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 55690-60-3 is helpful to your research.

Reference£º
Thiazole | C3H6431NS – PubChem,
Thiazole | chemical compound | Britannica

55690-60-3, Name is 5-Methoxybenzo[d]thiazole-2-thiol, molecular formula is C8H7NOS2, belongs to thiazole compound, is a common compound. In a patnet, assignee is Heike, Wulff55690-60-3, once mentioned the new application about 55690-60-3

Compositions of matter comprising 5-phenoxyalkoxypsoralen compounds and their method of synthesis and use. The compounds are useable to treat diseases or disorders in human or animal subjects, including autoimmune diseases. The compounds inhibit potassium channels, including the Kv1.3 channel and at least some of the therapeutic effects of such compounds may be due at least in part to potassium channel inhibition. In some embodiments, the compounds are more selective for certain potassium channels (e.g., Kv1.3 channels) than other potassium channels (e.g., Kv1.5 channels).

Compositions of matter comprising 5-phenoxyalkoxypsoralen compounds and their method of synthesis and use. The compounds are useable to treat diseases or disorders in human or animal subjects, including autoimmune diseases. The compounds inhibit potassium channels, including the Kv1.3 channel and at least some of the therapeutic effects of such compounds may be due at least in part to potassium channel inhibition. In some embodiments, the compounds are more selective for certain potassium channels (e.g., Kv1.3 channels) than other potassium channels (e.g., Kv1.5 channels).

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 55690-60-3, 55690-60-3

Reference£º
Thiazole | C3H6450NS – PubChem,
Thiazole | chemical compound | Britannica

55690-60-3, 5-Methoxybenzo[d]thiazole-2-thiol is a thiazole compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

55690-60-3, A mixture of 5-methoxy-1,3-benzothiazole-2-thiol (500 mg), thionyl chloride (2 mL) and DMF (1 drop) was stirred at 50 C. for 3 days. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture, and the obtained mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (211 mg).1H NMR (300 MHz, DMSO-d6) delta 3.84 (3H, s), 7.15 (1H, dd, J=9.0, 2.5 Hz), 7.53 (1H, d, J=2.5 Hz), 7.97 (1H, d, J=9.0 Hz).

The synthetic route of 55690-60-3 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Yamashita, Tohru; Kamata, Makoto; Hirose, Hideki; Murakami, Masataka; Fujimoto, Takuya; Ikeda, Zenichi; Yasuma, Tsuneo; Fujimori, Ikuo; Mizojiri, Ryo; Yukawa, Tomoya; US2011/263562; (2011); A1;,
Thiazole | C3H3NS – PubChem
Thiazole | chemical compound | Britannica