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Methyl 5-hydroxy-2,3-dimethylbenzoate is an organic compound with the chemical formula C10H12O3. It is a derivative of benzoic acid, featuring a hydroxyl group at the 5th carbon position, and methyl groups at the 2nd and 3rd carbon positions. methyl 5-hydroxy-2,3-dimethylbenzoate is a white crystalline solid and is soluble in organic solvents. It is synthesized by esterification of 5-hydroxy-2,3-dimethylbenzoic acid with methanol. Methyl 5-hydroxy-2,3-dimethylbenzoate has potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable compound for further research and development in these fields.

5628-58-0

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5628-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5628-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5628-58:
(6*5)+(5*6)+(4*2)+(3*8)+(2*5)+(1*8)=110
110 % 10 = 0
So 5628-58-0 is a valid CAS Registry Number.

5628-58-0Relevant academic research and scientific papers

Computational and Experimental Studies of Phthaloyl Peroxide-Mediated Hydroxylation of Arenes Yield a More Reactive Derivative, 4,5-Dichlorophthaloyl Peroxide

Camelio, Andrew M.,Liang, Yong,Eliasen, Anders M.,Johnson, Trevor C.,Yuan, Changxia,Schuppe, Alex W.,Houk,Siegel, Dionicio

, p. 8084 - 8095 (2015/09/01)

The oxidation of arenes by the reagent phthaloyl peroxide provides a new method for the synthesis of phenols. A new, more reactive arene oxidizing reagent, 4,5-dichlorophthaloyl peroxide, computationally predicted and experimentally determined to possess enhanced reactivity, has expanded the scope of the reaction while maintaining a high level of tolerance for diverse functional groups. The reaction proceeds through a novel "reverse-rebound" mechanism with diradical intermediates. Mechanistic insight was achieved through isolation and characterization of minor byproducts, determination of linear free energy correlations, and computational analysis of substituent effects of arenes, each of which provided additional support for the reaction proceeding through the diradical pathway.

NOVEL CYCLIC BENZIMIDAZOLE DERIVATIVES USEFUL AS ANTI-DIABETIC AGENTS

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Page/Page column 38, (2010/04/25)

Novel compounds of the structural formula (I) are activators of AMP-protein kinase and are useful in the treatment, prevention and suppression of diseases mediated by the AMPK-activated protein kinase. The compounds of the present invention are useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.

NOVEL CYCLIC BENZIMIDAZOLE DERIVATIVES USEFUL ANTI-DIABETIC AGENTS

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Page/Page column 79, (2010/05/13)

Novel compounds of the structural formula (I) are activators of AMP-protein kinase and are useful in the treatment, prevention and suppression of diseases mediated by the AMPK-activated protein kinase. The compounds of the present invention are useful in the treatment of Type 2 diabetes, hyperglycemia, Metabolic Syndrome, obesity, hypercholesterolemia, and hypertension

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