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11-Octadecynoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26543-37-3

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26543-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26543-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,4 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26543-37:
(7*2)+(6*6)+(5*5)+(4*4)+(3*3)+(2*3)+(1*7)=113
113 % 10 = 3
So 26543-37-3 is a valid CAS Registry Number.

26543-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl octadec-11-ynoate

1.2 Other means of identification

Product number -
Other names Methyl 11-octadecynoate

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:26543-37-3 SDS

26543-37-3Relevant academic research and scientific papers

Efficient synthesis of unsaturated 1-monoacyl glycerols for in meso crystallization of membrane proteins

Fu, Yu,Weng, Yue,Hong, Wen-Xu,Zhang, Qinghai

, p. 809 - 812 (2011/06/21)

A highly efficient synthesis of unsaturated 1-monoacyl glycerols was established to fulfill the pressing need for materials that form lipidic mesophases utilized in membrane protein crystallization. Georg Thieme Verlag Stuttgart.

Studies in pheromone biosynthesis: Preparation of 3H labelled precursors of Drosophila pheromones

Bricard,Kunesch

, p. 2547 - 2558 (2007/10/02)

Two synthetic schemes were designed giving access to tritium labelled potential precursors of Drosophila pheromones. An intermediate in the first scheme allowed the preparation of [3H]-labelled vaccenyl acetate.

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