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9-Octadecen-12-ynoic acid, methyl ester, (9Z)-, also known as methyl (9Z)-9-octadecen-12-ynoate, is a chemical compound with the molecular formula C19H32O2. It is a derivative of octadecenoic acid, featuring a triple bond between carbons 11 and 12, and a methyl ester group attached to the carboxylic acid. This unsaturated fatty acid is characterized by its 9Z configuration, indicating a cis double bond between carbons 9 and 10. It is commonly found in various plant oils and is used in the synthesis of specialty chemicals, such as surfactants and lubricants, due to its unique structure and properties.

2907-83-7

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2907-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2907-83-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2907-83:
(6*2)+(5*9)+(4*0)+(3*7)+(2*8)+(1*3)=97
97 % 10 = 7
So 2907-83-7 is a valid CAS Registry Number.

2907-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl octadec-9-en-12-ynoate

1.2 Other means of identification

Product number -
Other names Crepenynsaeuremethylester

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:2907-83-7 SDS

2907-83-7Relevant academic research and scientific papers

Synthesis and Biological Evaluation of Chlorinated Analogs of Leukotoxin Diol

Nilewski, Christian,Chapelain, Camille Le,Wolfrum, Susanne,Carreira, Erick M.

, p. 5602 - 5605 (2015/12/01)

This study documents that chlorinated analogs of leukotoxin diol 1, in which the vic-diol has been replaced with vic-chlorides (2), induce caspase 3 activity and apoptosis on HepG2 cells in a dose-dependent manner in analogy to the parent diol. This sugge

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