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2724-57-4

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2724-57-4 Usage

Uses

12-Methyltridecanoic Acid is a branched fatty acid found naturally in fish and in other Asian fermented foods.

Check Digit Verification of cas no

The CAS Registry Mumber 2724-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,2 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2724-57:
(6*2)+(5*7)+(4*2)+(3*4)+(2*5)+(1*7)=84
84 % 10 = 4
So 2724-57-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H28O2/c1-13(2)11-9-7-5-3-4-6-8-10-12-14(15)16/h13H,3-12H2,1-2H3,(H,15,16)

2724-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name isomyristic acid

1.2 Other means of identification

Product number -
Other names Tridecanoic acid, 12-methyl-

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:2724-57-4 SDS

2724-57-4Relevant articles and documents

A practical synthesis of long-chain iso-fatty acids (iso-C 12-C19) and related natural products

Richardson, Mark B.,Williams, Spencer J.

, p. 1807 - 1812 (2013/10/22)

A gram-scale synthesis of terminally-branched iso-fatty acids (iso-C 12-C19) was developed commencing with methyl undec-10-enoate (methyl undecylenate) (for iso-C12-C14) or the C15 and C16 lactones pentadecanolide (for iso-C 15-C17) and hexadecanolide (for iso-C18-C 19). Central to the approaches outlined is the two-step construction of the terminal isopropyl group through addition of methylmagnesium bromide to the ester/lactones and selective reduction of the resulting tertiary alcohols. Thus, the C12, C17 and C18 iso-fatty acids were obtained in three steps from commercially-available starting materials, and the remaining C13-C16 and C19 iso-fatty acids were prepared by homologation or recursive dehomologations of these fatty acids or through intercepting appropriate intermediates. Highlighting the synthetic potential of the iso-fatty acids and various intermediates prepared herein, we describe the synthesis of the natural products (S)-2,15-dimethylpalmitic acid, (S)-2-hydroxy-15-methylpalmitic acid, and 2-oxo-14-methylpentadecane.

Synthesis and Absolute Configuration of 2-Hydroxy-12-methyl Tridecanoic Acid

Balzer, Th.,Budzikiewicz, H.

, p. 1367 - 1368 (2007/10/02)

The synthesis of racemic 2-hydroxy-12-methyl tridecanoic acid is described.The absolute configuration of the two enantiomers has been determined by the method of Dale and Mosher. - Keywords: 2-Hydroxy-12-methyl Tridecanoic Acid, Absolute COnfiguration

Structure and biological activity of neopeptins A, B and C, inhibitors of fungal cell wall glycan synthesis

Ubukata,Uramoto,Uzawa,Isono

, p. 357 - 365 (2007/10/02)

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