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10178-35-5

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10178-35-5 Usage

General Description

(12Z)-Labda-8(17),12,14-triene-19-oic acid methyl ester is a diterpene compound found in various plants and has been shown to possess anti-inflammatory, antifungal, and anticancer properties. It has been isolated from several plant species and has been used in traditional medicine for its therapeutic properties. (12Z)-Labda-8(17),12,14-triene-19-oic acid methyl ester has been studied for its potential as a natural product for the development of new drugs, particularly for inflammatory and cancer-related conditions. Additionally, its chemical structure and biological activity make it a promising candidate for further research and potential future pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 10178-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10178-35:
(7*1)+(6*0)+(5*1)+(4*7)+(3*8)+(2*3)+(1*5)=75
75 % 10 = 5
So 10178-35-5 is a valid CAS Registry Number.

10178-35-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl ester of cis-communic acid

1.2 Other means of identification

Product number -
Other names Methylelliotinoat, Methylcommunat

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:10178-35-5 SDS

10178-35-5Relevant articles and documents

Syntheses and structural confirmations of members of a heterocycle- containing family of labdane diterpenoids

MacK, Daniel J.,Njardarson, Jon T.

, p. 1543 - 1547 (2013)

Building with berries! Several labdane natural products have been synthesized for the first time by the combination of a copper-catalyzed vinyl oxirane ring expansion reaction with an abundant, inexpensive, chiral natural source (juniper berries; see scheme). These expedient (1-5 step) syntheses have resulted in the structural confirmations of five natural products and one reassignment. Reagent-controlled oxidation and 1,3-diene isomerization results are also presented. Copyright

Anti-inflammatory constituents of topically applied crude drugs. II. Constituents and anti-inflammatory effect of Cryptomeria japonica D.Don

Shimizu,Tsuji,Shogawa,Fukumura,Tanaami,Hayashi,Arisawa,Morita

, p. 3967 - 3973 (2007/10/02)

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