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α-(3,4-dimethoxyphenyl)-α-methoxyacetate is a chemical compound with the molecular formula C11H14O5. It is an organic ester derived from α-methoxyacetic acid and 3,4-dimethoxyphenol. α-(3,4-dimethoxyphenyl)-α-methoxyacetate is characterized by the presence of two methoxy groups attached to the phenyl ring and one methoxy group attached to the acetate moiety. It is a colorless to pale yellow liquid with a molecular weight of 226.23 g/mol. The compound is used in various applications, including pharmaceuticals and agrochemicals, due to its potential biological activity and chemical reactivity. Its synthesis typically involves the esterification of α-methoxyacetic acid with 3,4-dimethoxyphenol, and it can be further functionalized or used as a building block in the synthesis of more complex molecules.

83831-76-9

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83831-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83831-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,3 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83831-76:
(7*8)+(6*3)+(5*8)+(4*3)+(3*1)+(2*7)+(1*6)=149
149 % 10 = 9
So 83831-76-9 is a valid CAS Registry Number.

83831-76-9Relevant academic research and scientific papers

Amides for the treatment of atherosclerosis

-

, (2008/06/13)

This invention provides amide compounds as inhibitors of acyl-Coenzyme A: cholesterol O-acyltransferase (ACAT), pharmaceutical compositions containing such compounds, processes for the preparation of such compounds, and the use of such compounds as antihypercholesterolemic and/or antiatherosclerotic agents.

UTILIZATION OF METHYLTHIOMETHYL p-TOLYL SULFONE IN ORGANIC SYNTHESIS

Ogura, Katsuyuki,Yahata, Nobuhiro,Hashizume, Kimitoshi,Tsuyama, Koichi,Takahashi, Kazumasa,Iida, Hirotada

, p. 767 - 770 (2007/10/02)

Methylthiomethyl p-tolyl sulfone was found to be one of the useful reagents for preparation of various organic compounds such as S-methyl α-ketocarbothioates, carboxylic esters, five- and six-membered cycloalkanones, and α-methoxy-α-arylacetic esters.

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