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5,6-dimethyl-2-hydroxybenzoic acid is an organic compound with the chemical formula C9H10O4. It is a derivative of benzoic acid, featuring two methyl groups at the 5th and 6th carbon positions and a hydroxyl group at the 2nd carbon position. 5,6-dimethyl-2-hydroxybenzoic acid is a white crystalline solid and is soluble in organic solvents such as ethanol and acetone. It has various applications in the chemical industry, including the synthesis of pharmaceuticals, dyes, and other organic compounds. Due to its unique structure, it can act as a building block for more complex molecules, making it a valuable intermediate in organic synthesis.

5628-59-1

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5628-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5628-59-1 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 5628-59:
(6*5)+(5*6)+(4*2)+(3*8)+(2*5)+(1*9)=111
111 % 10 = 1
So 5628-59-1 is a valid CAS Registry Number.

5628-59-1Downstream Products

5628-59-1Relevant academic research and scientific papers

Palladium-catalyzed ortho-C-H hydroxylation of benzoic acids

Luo, Feihua,He, Shuhua,Gou, Quan,Chen, Jinyang,Zhang, mingzhong

, (2021/10/06)

A simple Pd(OAc)2 catalyzed ortho-hydroxylation of benzoic acids using TBHP as the sole oxidant has been explored. This protocol features relatively broad substrate scope and operational simplicity. The compatibility of ortho-substituted substrates is an effective complement to the previous ortho-hydroxylation reaction.

Synthesis of o-Carboxyarylacrylic Acids by Room Temperature Oxidative Cleavage of Hydroxynaphthalenes and Higher Aromatics with Oxone

Parida, Keshaba Nanda,Moorthy, Jarugu Narasimha

, p. 8354 - 8360 (2015/09/01)

A simple procedure for the synthesis of a variety of o-carboxyarylacrylic acids has been developed with Oxone (2KHSO5·KHSO4·K2SO4); the oxidation reaction involves the stirring of methoxy/hydroxy-substituted naphthalenes, phenanthrenes, anthracenes, etc. with Oxone in an acetonitrile-water mixture (1:1, v/v) at rt. Mechanistically, the reaction proceeds via initial oxidation of naphthalene to o-quinone, which undergoes cleavage to the corresponding o-carboxyarylacrylic acid. The higher aromatics are found to yield carboxymethyl lactones derived from the initially formed o-carboxyarylacrylic acids.

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