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5129-57-7

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5129-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5129-57-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,2 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5129-57:
(6*5)+(5*1)+(4*2)+(3*9)+(2*5)+(1*7)=87
87 % 10 = 7
So 5129-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H28O2/c1-13(2)11-9-7-5-4-6-8-10-12-14(15)16-3/h13H,4-12H2,1-3H3

5129-57-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 11-methyldodecanoate

1.2 Other means of identification

Product number -
Other names 11-Methyllauric acid methyl ester

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:5129-57-7 SDS

5129-57-7Relevant articles and documents

Long-Chain Alkyl Cyanides: Unprecedented Volatile Compounds Released by Pseudomonas and Micromonospora Bacteria

Montes Vidal, Diogo,von Rymon-Lipinski, Anna-Lena,Ravella, Srinivasa,Groenhagen, Ulrike,Herrmann, Jennifer,Zaburannyi, Nestor,Zarbin, Paulo H. G.,Varadarajan, Adithi R.,Ahrens, Christian H.,Weisskopf, Laure,Müller, Rolf,Schulz, Stefan

supporting information, p. 4342 - 4346 (2017/04/03)

The analysis of volatiles from bacterial cultures revealed long-chain aliphatic nitriles, a new class of natural products. Such nitriles are produced by both Gram-positive Micromonospora echinospora and Gram-negative Pseudomonas veronii bacteria, although the structures differ. A variable sequence of chain elongation and dehydration in the fatty acid biosynthesis leads to either unbranched saturated or unsaturated nitriles with an ω?7 double bond, such as (Z)-11-octadecenenitrile, or methyl-branched unsaturated nitriles with the double bond located at C-3, such as (Z)-13-methyltetradec-3-enenitrile. The nitrile biosynthesis starts from fatty acids, which are converted into their amides and finally dehydrated. The structures and biosyntheses of the 19 naturally occurring compounds were elucidated by mass spectrometry, synthesis, and feeding experiments with deuterium-labeled precursors. Some of the nitriles showed antimicrobial activity, for example, against multiresistant Staphylococcus aureus strains.

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