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(1S,8aβ)-Decahydro-1β-hydroxy-4aα-methyl-α,8-dimethylene-2α-naphthaleneacetic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81373-87-7

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81373-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81373-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,7 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81373-87:
(7*8)+(6*1)+(5*3)+(4*7)+(3*3)+(2*8)+(1*7)=137
137 % 10 = 7
So 81373-87-7 is a valid CAS Registry Number.

81373-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6α-hydroxycostic acid methyl ester

1.2 Other means of identification

Product number -
Other names 2-((1S,2S,4aR,8aS)-1-Hydroxy-4a-methyl-8-methylene-decahydro-naphthalen-2-yl)-acrylic 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:81373-87-7 SDS

81373-87-7Relevant academic research and scientific papers

EUDESMANE SESQUITERPENES FROM EUPATORIUM QUADRANGULARE

Gonzalez, Antonio G.,Barrera, Jaime Bermejo,Hernandez, Angel C. Janes,Rosas, Francisco Estevez,Dominguez, Xorge A.

, p. 1847 - 1848 (1985)

The aerial part of Eupatorium quadrangulare afforded in addition to known compounds, a possible biosynthetic intermediate quadrangulin A, of the eudesmanolides found in this species. Key Word Index - Eupatorium quadrangulare; Compositae; sesquiterpene lactones; eudesmanolides.

Antimony Trichloride Catalysed Reactions on Cyclocostunolides

Kalsi, P. S.,Khurana, Sarita

, p. 1145 - 1146 (2007/10/02)

γ-Hydroxy esters (III and IV) derived from α- and β-cyclocostunolides (I) and (II), respectively undergo intramolecular transesterification on reaction with antimony trichloride in methanol.In the case of II this reaction is attended with a double bond shift.Unlike I, II undergoes an addition to the C4-exocyclic olefin.

Antimony Trichloride Catalysed Reactions on Terpenoids

Kalsi, P. S.,Dhillon, R. S.,Kaur, Satinder,Gupta, Rachna

, p. 986 - 988 (2007/10/02)

Unlike homoallylic alcohols which undergo addition to the olefin, allylic alcohols undergo substitution reaction in antimony trichloride catalysed reaction.This reaction involves a carbonium ion mechanism.However, there is a high degree of selectivity in the formation of the reaction products which have some differences in their stabilities.In case of lactones, products arising from alkyl oxygen and acyl oxygen cleavages are formed depending on the stability of the ions obtained by these cleavages.

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