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7-keto dehydroabietic acid methyl ester is a complex organic compound derived from abietic acid, a diterpene found in the resin of coniferous trees. It is characterized by a carbonyl group at the 7-position and a methyl ester functional group. 7-keto dehydroabietic acid methyl ester is of interest in the field of organic chemistry and has potential applications in the synthesis of various chemicals and materials. Its structure and properties make it a valuable intermediate in the production of pharmaceuticals, fragrances, and other specialty chemicals. The compound's unique features also make it a subject of study for researchers exploring the chemical diversity of natural products and their derivatives.

5395-88-0

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5395-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5395-88-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5395-88:
(6*5)+(5*3)+(4*9)+(3*5)+(2*8)+(1*8)=120
120 % 10 = 0
So 5395-88-0 is a valid CAS Registry Number.

5395-88-0Downstream Products

5395-88-0Relevant academic research and scientific papers

Electrooxidative Functionalizations of Dehydroabietic Acid

Uneyama, Kenji,Katayama, Tatsuo,Torii, Sigeru

, p. 3043 - 3044 (2007/10/02)

Dehydroabietic acid methyl ester (1) was converted into 7-acetoxydehydroabietic acid methyl ester by direct electrooxidation in acetic acid and 7-oxodehydroabietic acid methyl ester by ruthenium dioxide-mediated oxidation.Non-Kolbe type electrodecarboxylation of 1 resulted in the introduction of a double bond into the ring A of 1.

REGIOSELECTIVE REACTIONS OF ABIETIC ACID METHYL ESTER

Escudero, Javier,Marquez, Cecilio,Rabanal, Rosa Ma,Valverde, S.

, p. 3167 - 3170 (2007/10/02)

Ozonolysis of abietic acid methyl ester 1 in the presence of mercuric acetate afforded the 13,14-seco-derivative in fair yield (50percent).Selenium dioxide oxidation of 1 in t-butanol gave 9-α-hydroxy-abietic acid methyl ester 6, dehydroabietic acid methyl ester 4 and its 7α-hydroxy-derivative 4b.

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