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Podocarpa-8,11,13-trien-19-oic acid methyl ester is a naturally occurring organic compound derived from podocarpic acid, a diterpenoid found in plants of the Podocarpaceae family. This specific chemical is characterized by its unique molecular structure, featuring a tricyclic diterpene core with three double bonds at the 8, 11, and 13 positions, and a carboxylic acid group at the 19 position. The methyl ester functional group is attached to the carboxylic acid, making it a derivative of podocarpic acid. Podocarpa-8,11,13-trien-19-oic acid methyl ester has been studied for its potential biological activities, including anti-inflammatory and anticancer properties, and is of interest to researchers in the field of natural product chemistry and pharmacology.

2651-34-5

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2651-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2651-34-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2651-34:
(6*2)+(5*6)+(4*5)+(3*1)+(2*3)+(1*4)=75
75 % 10 = 5
So 2651-34-5 is a valid CAS Registry Number.

2651-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethylphenanthrene-1-carboxylate

1.2 Other means of identification

Product number -
Other names (1S,4aS,10aR)-1,4a-Dimethyl-1,2,3,4,4a,9,10,10a-octahydro-phenanthrene-1-carboxylic acid methyl ester

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:2651-34-5 SDS

2651-34-5Upstream product

2651-34-5Relevant academic research and scientific papers

Stereoselective intramolecular 6-exo-Heck reaction : A facile synthetic route to podocarpa-8,11,13-triene and diterpenoid resin acids intermediates

Mukhopadhyaya, Jayanta K.,Ghosh, Ajit K.,Ghatak, Usha Ranjan

, p. 835 - 837 (2007/10/03)

Intramolecular Heck reaction of the olefins 1a-c in the presence of sodium formate affords ca 3:1 mixtures of the respective trans- and cis-octahydrophenanthrenes 3a-c and 4a-c. Similar reaction of the olefmic ester 2 provides a 70:30 mixture of (±)-methyl desisopropyldehydroabietate 6 and (±)10-epi-methyl desoxypodocarpate 7.

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