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Abieta-8,11,13-triene-19-oic acid is a naturally occurring diterpenoid compound, characterized by its unique molecular structure featuring three double bonds at the 8th, 11th, and 13th carbon positions, and a carboxylic acid functional group at the 19th carbon position. This organic compound is derived from the abietane class of diterpenes, which are widely found in coniferous plants and have various biological activities. It is known for its potential anti-inflammatory, antimicrobial, and anticancer properties, making it a subject of interest in pharmaceutical research. The compound's specific structure and biological activities suggest its potential use in the development of new drugs and therapeutic agents.

5155-70-4

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5155-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5155-70-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,5 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5155-70:
(6*5)+(5*1)+(4*5)+(3*5)+(2*7)+(1*0)=84
84 % 10 = 4
So 5155-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O2/c1-13(2)14-6-8-16-15(12-14)7-9-17-19(16,3)10-5-11-20(17,4)18(21)22/h6,8,12-13,17H,5,7,9-11H2,1-4H3,(H,21,22)/t17?,19-,20+/m1/s1

5155-70-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,4aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 13-ISOPROPYLPODOCARPA-8,11,13-TRIEN-16-OIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5155-70-4 SDS

5155-70-4Upstream product

5155-70-4Downstream Products

5155-70-4Relevant academic research and scientific papers

Oxonitriles: Multicomponent Grignard addition-alkylations

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

, p. 1126 - 1129 (2007/10/03)

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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