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1731-86-8

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1731-86-8 Usage

Description

METHYL UNDECANOATE, also known as a fatty acid methyl ester of undecanoic acid, is an organic compound that belongs to the class of esters. It is characterized by its ester functional group, which is formed by the reaction between a carboxylic acid and an alcohol. METHYL UNDECANOATE possesses unique properties that make it suitable for various applications across different industries.

Uses

Used in Polymer Industry:
METHYL UNDECANOATE is used as a plasticizer in polymers for improving their flexibility, workability, and processability. Its ester structure allows it to interact with polymer chains, reducing intermolecular forces and enhancing the overall plasticity of the material.
Used in Aroma and Flavor Chemicals Industry:
METHYL UNDECANOATE is used as a fragrance agent in the aroma and flavor chemicals industry due to its pleasant odor and ability to impart specific scents to various products. Its compatibility with a wide range of substances makes it a versatile ingredient in the formulation of perfumes, cosmetics, and other fragranced products.

Synthesis Reference(s)

The Journal of Organic Chemistry, 53, p. 3158, 1988 DOI: 10.1021/jo00249a007

Check Digit Verification of cas no

The CAS Registry Mumber 1731-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1731-86:
(6*1)+(5*7)+(4*3)+(3*1)+(2*8)+(1*6)=78
78 % 10 = 8
So 1731-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O2/c1-3-4-5-6-7-8-9-10-11-12(13)14-2/h3-11H2,1-2H3

1731-86-8 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L05939)  Methyl undecanoate, 99%   

  • 1731-86-8

  • 5g

  • 196.0CNY

  • Detail
  • Alfa Aesar

  • (L05939)  Methyl undecanoate, 99%   

  • 1731-86-8

  • 25g

  • 681.0CNY

  • Detail
  • Sigma-Aldrich

  • (47147)  Methylundecanoate  certified reference material, TraceCERT®

  • 1731-86-8

  • 47147-100MG

  • 816.66CNY

  • Detail

1731-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl undecanoate

1.2 Other means of identification

Product number -
Other names Methyl undecanoate

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:1731-86-8 SDS

1731-86-8Relevant articles and documents

Intermolecular Radical Addition of 1-Alkoxyalkyl Radicals to Vinyl Derivatives

Nishiyama, Yutaka,Yamamoto, Hisayuki,Nakata, Shinji,Shii, Yasutaka

, p. 841 - 844 (1993)

1-Alkoxyalkyl radicals 1R2(OR3)C>, which were generated from 1-alkoxy-1-(phenylseleno)alkanes 1R2C(OR3)SePh> and n-Bu3SnH in the precence of AIBN, participate effectively in intermolecular addition to vinyl compounds bearing electron-withdrawing or radical stabilizing substituents to give the corresponding ethers in moderate to good yields.

Silylene-Bridged Tetranuclear Palladium Cluster as a Catalyst for Hydrogenation of Alkenes and Alkynes

Yanagisawa, Chikako,Yamazoe, Seiji,Sunada, Yusuke

, p. 169 - 173 (2020/10/29)

A planar tetranuclear palladium cluster was obtained from the reaction of a cyclotetrasilane with [Pd(CNtBu)2]3. Single-crystal X-ray diffraction analysis and DFT calculations revealed that the tetranuclear framework of the cluster was supported effectively by the bridging organosilylene ligand. Although [Pd(CNtBu)2]3 as well as mononuclear palladium bis(silyl) complex, cis-Pd(SiMePh2)2(CNtBu)2, do not act as the effective catalyst, the planar tetranuclear palladium cluster acts as an efficient catalyst for the hydrogenation of alkenes and alkynes including sterically hindered tri- and tetra-substituted alkenes.

C-C Bond Cleavage of Unactivated 2-Acylimidazoles

Xin, Hai-Long,Pang, Bo,Choi, Jeesoo,Akkad, Walaa,Morimoto, Hiroyuki,Ohshima, Takashi

, p. 11592 - 11606 (2020/10/23)

2-Acylimidazoles are widely used as post-Transformable carboxylic acid equivalents in chemoselective and enantioselective reactions. Their transformations, however, require pretreatment with highly reactive, toxic methylating reagents to facilitate C-C bond cleavage. Here, we demonstrate that such pretreatment can be avoided and the C-C bond cleaved under neutral conditions without the use of additional reagents or catalysts. The scope of the reaction, including the use of products reported in the literature as substrates, and some mechanistic insights are described.

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