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Rac-abieta-8,11,13-trien-18-oic acid is a naturally occurring triterpenoid compound, which belongs to the abietane family of diterpenes. It is characterized by its unique molecular structure, featuring a tricyclic arrangement of carbon atoms with three double bonds at the 8th, 11th, and 13th positions, and a carboxylic acid functional group at the 18th position. rac-abieta-8,11,13-trien-18-oic acid is found in various plant species, particularly in the resin of coniferous trees, and has been studied for its potential biological activities, such as anti-inflammatory and antimicrobial properties. The "rac" prefix in its name indicates that it is a racemic mixture, meaning it consists of equal parts of both the R and S enantiomers, which are mirror images of each other. Rac-abieta-8,11,13-trien-18-oic acid is of interest to researchers due to its potential applications in pharmaceuticals and natural product chemistry.

6980-63-8

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6980-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6980-63-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,8 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6980-63:
(6*6)+(5*9)+(4*8)+(3*0)+(2*6)+(1*3)=128
128 % 10 = 8
So 6980-63-8 is a valid CAS Registry Number.

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6980-63-8Downstream Products

6980-63-8Relevant academic research and scientific papers

Oxonitriles: Multicomponent Grignard addition-alkylations

Fleming, Fraser F.,Zhang, Zhiyu,Wang, Qunzhao,Steward, Omar W.

, p. 1126 - 1129 (2004)

Three at a time: Sequential carbonyl addition, chelation-controlled conjugate addition, and alkylation triggers the multicomponent assembly of diverse nitriles. The chelation-controlled conjugate addition-alkylation installs three new stereocenters (see scheme), thereby generating substituted nitriles that are ideal terpenoid precursors as illustrated in the synthesis of epi-dehydroabietic acid.

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