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Methyl 3-ethoxy-4-hydroxycinnamate is a chemical compound belonging to the class of cinnamic acid derivatives, characterized by a hydroxyl group at the 4-position and an ethoxy group at the 3-position. This organic molecule is a type of ester, formed by the reaction of 3-ethoxy-4-hydroxy-cinnamic acid with methanol. It is known for its potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various pharmaceuticals and as a component in the formulation of certain cosmetics. The compound's structure and properties make it a versatile building block in organic synthesis, with potential uses in the development of new drugs and other chemical products.

4657-38-9

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4657-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4657-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,5 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4657-38:
(6*4)+(5*6)+(4*5)+(3*7)+(2*3)+(1*8)=109
109 % 10 = 9
So 4657-38-9 is a valid CAS Registry Number.

4657-38-9Downstream Products

4657-38-9Relevant academic research and scientific papers

OLEFIN SATURATION AND ACID REDUCTION OF 3,4-DIMETHOXYCINNAMIC ACID AND DERIVATIVES BY PHANEROCHAETE CHRYSOSPORIUM

Enoki, Akio,Yajima, Yasuo,Gold, Michael H.

, p. 1543 - 1546 (1981)

The white rot fungus Phanerochaete chrysosporium metabolized 3,4-dimethoxycinnamic acid in shaking and nitrogen sufficient cultures.Metabolites identified included 3-(3,4-dimethoxyphenyl)propionic acid, dimethoxycinnamyl alcohol and 3-(3,4-dimethoxyphenyl)-1-propanol.Significantly smaller amounts of veratryl and vanillyl alcohol were also present.The abundance of the propionic acid and the propanol as metabolic products indicate that olefin saturation and acid reduction are important reactions catalysed under these conditions.Metabolites identified from the metabolism of 3-(3,4-dimethoxyphenyl)-propionic acid included the above 1-propanol as well as veratryl and vanillyl alcohol; the identification of these benzyl alcohol derivatives as metabolites suggests that α,β-bond cleavage of this substrate was preceded by alkane hydroxylation at the α-position.Key Word Index-Phanerochaete chrysosporium; basidiomycete; dimethoxycinnamic acid; ferulic acid; veratryl alcohol; acid reduction; olefin saturation; metabolism

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