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Methyl-trans-deisopropyldehydroabietate is a naturally occurring organic compound derived from the resin of coniferous trees, specifically from the genus Abies, commonly known as fir trees. It is a diterpene, a type of terpene with a molecular formula of C20H28O2, and is characterized by its unique chemical structure, which includes a methyl group and a dehydroabietane skeleton. Methyl-trans deisopropyldehydroabietate has been studied for its potential applications in various fields, such as pharmaceuticals and fragrances, due to its biological activities and unique scent profile. Methyl-trans-deisopropyldehydroabietate is also of interest to researchers in the field of natural product chemistry, as it represents a complex and intriguing molecule that can provide insights into the biosynthesis and ecological roles of diterpenes in plants.

3650-04-2

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3650-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3650-04-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3650-04:
(6*3)+(5*6)+(4*5)+(3*0)+(2*0)+(1*4)=72
72 % 10 = 2
So 3650-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H24O2/c1-17-11-6-12-18(2,16(19)20-3)15(17)10-9-13-7-4-5-8-14(13)17/h4-5,7-8,15H,6,9-12H2,1-3H3/t15?,17-,18+/m1/s1

3650-04-2SDS

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 methyl 10β-methyl-13 deisopropyldehydroabietate

1.2 Other means of identification

Product number -
Other names trans methyl podocarpa-8,11,13-trien-15-oate

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:3650-04-2 SDS

3650-04-2Upstream product

3650-04-2Relevant 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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