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2-Hexylcyclopropane-1-decanoic acid methyl ester is a complex organic compound with the molecular formula C19H36O2. It is a derivative of decanoic acid, featuring a cyclopropane ring and a hexyl group attached to the second carbon. This ester is formed by the methylation of 2-hexylcyclopropane-1-decanoic acid, where a methyl group replaces the hydroxyl group of the carboxylic acid. The compound is characterized by its unique structure, which includes a three-membered carbon ring (cyclopropane) and a six-carbon alkyl chain (hexyl). It is likely to be found in the field of organic chemistry, potentially used in the synthesis of pharmaceuticals, fragrances, or other specialty chemicals due to its specific structural features.

5965-63-9

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5965-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5965-63-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5965-63:
(6*5)+(5*9)+(4*6)+(3*5)+(2*6)+(1*3)=129
129 % 10 = 9
So 5965-63-9 is a valid CAS Registry Number.

5965-63-9SDS

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 11,12-methyleneoctadecanoate methyl ester

1.2 Other means of identification

Product number -
Other names 11,12-Methylenoctadecanomethylat

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:5965-63-9 SDS

5965-63-9Downstream Products

5965-63-9Relevant academic research and scientific papers

Bioactive lipids from the sponge Spirastrella abata

Jang, Kyoung Hwa,Lee, Yoonyeong,Sim, Chung J.,Oh, Ki-Bong,Shin, Jongheon

supporting information; experimental part, p. 1078 - 1081 (2012/03/26)

Three sphingosine 4-sulfates (1-3) and a lysophosphatidylglycerol (4) were isolated from the Korean sponge Spirastrella abata. The structures of these compounds were determined based on the combined results of spectroscopic analyses. Based on the results

An Unexpected Reversal of Fluorine Substituent Effects in the Biomethylenation of Two Positional Isomers: A Serendipitous Discovery

Buist, Peter H.,Pon, Robert A.

, p. 6240 - 6241 (2007/10/02)

The mechanism of biological cyclopropyl fatty acid biosynthesis as it occurs in Lactobacillus plantarum has been probed using fluorine substituent effects.It has been shown that the pattern of rate retardations induced by homoallylic fluorine substitution is numerically the same but opposite in sense for two series of olefinic fatty acid substrates bearing the double bond at either the 9- or the 11-position.

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