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37056-34-1

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37056-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37056-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,5 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37056-34:
(7*3)+(6*7)+(5*0)+(4*5)+(3*6)+(2*3)+(1*4)=111
111 % 10 = 1
So 37056-34-1 is a valid CAS Registry Number.

37056-34-1SDS

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 8-cyanooctanoic acid

1.2 Other means of identification

Product number -
Other names Nonandisaeuremononitril

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:37056-34-1 SDS

37056-34-1Relevant articles and documents

SELECTIVE EXTRACTION OF AN OMEGA-FUNCTIONALIZED ACID AFTER OXIDATIVE CLEAVAGE OF AN UNSATURATED FATTY ACID AND DERIVATIVES

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Paragraph 0050; 0051; 0052, (2015/11/18)

The invention relates to a process for the selective extraction of a reaction product, derived from an oxidative cleavage of an unsaturated fatty acid or of an ester derivative or of an unsaturated nitrile derivative, said reaction product being an ω-functionalized acid from among C6 to C15 diacids, acid esters and acid nitriles, using as selective extraction solvent a composition comprising a mixture of water and of C1-C4 carboxylic acid. The invention also relates to the use of said process and of the extraction solvent composition for the preparation of C6 to C15 amino acid, diacid or acid ester monomers for the preparation of polycondensation polymers, in particular polyamides.

Transformation of peroxide products of olefin ozonolysis under treatment with hydroxylamine and semicarbazide hydrochlorides in acetic acid

Ishmuratov,Legostaeva,Garifullina,Botsman,Muslukhov,Tolstikov

, p. 1075 - 1081 (2015/02/02)

Hydrochlorides of hydroxylamine and semicarbazide efficiently reduce peroxide products of olefin ozonolysis in a system CH2Cl2-AcOH leading to the formation of carboxylic acids and their derivatives. The application of water as the solvent component favors the increase in the fraction of nitrogen-containing organic compounds (semicarbazones, keto- and aldoximes, nitriles) and reduction in the yield of carboxylic acids.

Polar Effects in Free-radical Reactions; Reductive Alkylation of Olefins Conjugated with Electron-withdrawing Groups: Kinetics and Mechanism

Citterio, Attilio,Minisci, Francesco,Serravalle, Marco

, p. 2174 - 2189 (2007/10/02)

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