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13150-81-7

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13150-81-7 Usage

General Description

2,6-DIMETHYLDECANE is a chemical compound that belongs to the class of organic alkanes. It has a molecular formula of C12H26 and a molecular weight of 170.33 g/mol. The compound is a colorless liquid at room temperature and is insoluble in water. It is primarily used as a solvent in various industrial applications, such as in the manufacturing of paints, coatings, and adhesives. 2,6-DIMETHYLDECANE is also used as a fuel additive and in the production of flavors and fragrances. It is considered to be relatively low in toxicity and is not known to pose significant health risks at normal levels of exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 13150-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13150-81:
(7*1)+(6*3)+(5*1)+(4*5)+(3*0)+(2*8)+(1*1)=67
67 % 10 = 7
So 13150-81-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H26/c1-5-6-9-12(4)10-7-8-11(2)3/h11-12H,5-10H2,1-4H3

13150-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-DIMETHYLDECANE

1.2 Other means of identification

Product number -
Other names 2,6-dimethyl-decane

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:13150-81-7 SDS

13150-81-7Downstream Products

13150-81-7Relevant articles and documents

Iron-catalysed allylation-hydrogenation sequences as masked alkyl-alkyl cross-couplings

Bernauer, Josef,Wu, Guojiao,Von Wangelin, Axel

, p. 31217 - 31223 (2019/10/19)

An iron-catalysed allylation of organomagnesium reagents (alkyl, aryl) with simple allyl acetates proceeds under mild conditions (Fe(OAc)2 or Fe(acac)2, Et2O, r.t.) to furnish various alkene and styrene derivatives. Mechanistic studies indicate the operation of a homotopic catalyst. The sequential combination of such iron-catalysed allylation with an iron-catalysed hydrogenation results in overall C(sp3)-C(sp3)-bond formation that constitutes an attractive alternative to challenging direct cross-coupling protocols with alkyl halides.

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