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(2alpha,15R)-12-chloro-2,16-dihydroxyabieta-8(14),9(11),12-trien-18-oic acid is a complex chemical compound that belongs to the class of abieta-8(14),9(11),12-trien-18-oic acid derivatives. It features a chloro group and multiple hydroxyl groups, with a specific stereochemical arrangement of 2alpha,15R. This unique structure may endow it with biological activity and potential applications in pharmaceutical research, as it could interact with biological systems or be modified to develop pharmaceutical agents.

88147-76-6

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88147-76-6 Usage

Uses

Used in Pharmaceutical Research:
(2alpha,15R)-12-chloro-2,16-dihydroxyabieta-8(14),9(11),12-trien-18-oic acid is used as a research compound for exploring its potential biological activity and interactions with biological systems. Its unique structure may allow for the development of new pharmaceutical agents or the modification of existing ones to enhance their efficacy.
Further research and exploration of the properties and potential applications of (2alpha,15R)-12-chloro-2,16-dihydroxyabieta-8(14),9(11),12-trien-18-oic acid are necessary to fully understand its capabilities and maximize its utility in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 88147-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,4 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88147-76:
(7*8)+(6*8)+(5*1)+(4*4)+(3*7)+(2*7)+(1*6)=166
166 % 10 = 6
So 88147-76-6 is a valid CAS Registry Number.

88147-76-6Upstream product

88147-76-6Downstream Products

88147-76-6Relevant academic research and scientific papers

Studies related to biological detoxification of kraft pulp mill effluent. VII. The biotransformation of 12-chlorodehydroabietic acid with Mortierella isabellina

Kutney,Hewitt,Salisbury,et al.

, p. 2191 - 2197 (1983)

A detailed study of the biodegradation of one of the fish-toxic chlorinated resin acids, 12-chlorodehydroabietic acid (3), is discussed. When 3 is exposed to the fungus Mortierella isabellina, it is converted into the monohydroxylated metabolites 2α-hydroxy-12-chlorodehydroabietic acid (5) and 16-hydroxy-12-chlorodehydroabietic acid (8) after short-term (26 h) incubation, and into the 2α, 16-dihydroxy derivatives 11 and 14 after 96 h incubation. These metabolites show low levels of toxicity to fish.

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