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132185-84-3

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132185-84-3 Usage

Uses

(2R,4aR,8aS)-Decahydro-8a-hydroxy-4a-methyl-α,8-bis(methylene)-2-naphthaleneacetic acid is extracted from the roots of Saussurea lappa, and Laggera pterodonta, may have anti-viral properties and used in traditional chinese medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 132185-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132185-84:
(8*1)+(7*3)+(6*2)+(5*1)+(4*8)+(3*5)+(2*8)+(1*4)=113
113 % 10 = 3
So 132185-84-3 is a valid CAS Registry Number.

132185-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2R,4aR,8aS)-8a-Hydroxy-4a-methyl-8-methylenedecahydro-2-napht halenyl]acrylic acid

1.2 Other means of identification

Product number -
Other names -

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:132185-84-3 SDS

132185-84-3Upstream product

132185-84-3Downstream Products

132185-84-3Relevant articles and documents

Eudesmane and megastigmane glucosides from Laggera alata

Zheng, Qunxiong,Xu, Zhaojun,Sun, Xianfeng,Yao, Wei,Sun, Handong,Cheng, Christopher H. K.,Zhao, Yu

, p. 835 - 839 (2007/10/03)

Four eudesmane glucosides, alatosides A-D (1-4), and one megastigmane glucoside, alatoside E (5), were isolated from the BuOH fraction of Laggera alata along with six known compounds. Structures of the new compounds were elucidated by a combination of chemical and spectroscopic methods. Alatosides A-E were characterized as: 1α-O-(β-D-glucopyranosyloxyl)-7-epi-eudesma-11-en-2β, 4α-diol (1), 2β-O-(β-D-glucopyranosyloxyl)-eudesma-4α-hydroxyl-11(13)- en-12-oic-acid (2), 5β-O-β-D-glucopyranosyloxyl)-eudesma-4(15), 11(13)-dien-12-oic-acid (3), 5α-O-(β-D-glucopyranosyloxyl)-eudesma-3,11 (13)-dien-12-oic acid (4) and 3β-O-(β-D-glucopyranosyloxyl)-megastigma-9-one (5), respectively. Based on the chemical characteristics of eudesmane derivatives isolated from the Laggera genus, it was suggested that there are probably two different biogenetic pathways for these secondary metabolites in this genus.

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