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1072-16-8

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1072-16-8 Usage

General Description

2,7-Dimethyloctane is a chemical compound with the molecular formula C10H22. It is a colorless liquid with a faint odor and is insoluble in water. 2,7-Dimethyloctane is primarily used as a solvent in various industries, including the production of paints, coatings, and adhesives. It is also used as an intermediate in the synthesis of other organic compounds. The chemical is flammable and should be handled with care, as it can pose a fire hazard. It is important to follow safety guidelines when working with 2,7-Dimethyloctane to avoid exposure and potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 1072-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1072-16:
(6*1)+(5*0)+(4*7)+(3*2)+(2*1)+(1*6)=48
48 % 10 = 8
So 1072-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H22/c1-9(2)7-5-6-8-10(3)4/h9-10H,5-8H2,1-4H3

1072-16-8 Well-known Company Product Price

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  • Alfa Aesar

  • (B21646)  2,7-Dimethyloctane, 98%   

  • 1072-16-8

  • 1g

  • 336.0CNY

  • Detail
  • Alfa Aesar

  • (B21646)  2,7-Dimethyloctane, 98%   

  • 1072-16-8

  • 5g

  • 1337.0CNY

  • Detail

1072-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-DIMETHYLOCTANE

1.2 Other means of identification

Product number -
Other names 2,5-DIMETHYLOXAZOLE-4-CARBALDEHYDE

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:1072-16-8 SDS

1072-16-8Related news

Shock tube and modeling study of 2,7-DIMETHYLOCTANE (cas 1072-16-8) pyrolysis and oxidation07/25/2019

High molecular weight iso-paraffinic molecules are found in conventional petroleum, Fischer–Tropsch (FT), and other alternative hydrocarbon fuels, yet fundamental combustion studies on this class of compounds are lacking. In the present work, ignition delay time measurements in 2,7-dimethylocta...detailed

1072-16-8Relevant articles and documents

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Davies,Dixon,Jones

, p. 1916,1919 (1930)

-

Mammalian exocrine secretions. XVII: chemical characterization of preorbital secretion of male suni, Neotragus moschatus.

Stander,Burger,Le, Roux M

, p. 89 - 101 (2002)

Gas chromatographic and gas chromatographic-mass spectrometric techniques were employed to identify 83 compounds, including alkanes, alkenes, aldehydes, 2-methylalkanes, carboxylic acids, 1-alkyl formates and alken-1-yl formates, benzoic acid, and cholest

Scott,Decicco

, p. 2663,2664,2666 (1976)

Ultrasound promoted Wurtz coupling of alkyl bromides and dibromides

Vandenburg, Daniel,Price, Gareth J.

experimental part, p. 5 - 8 (2012/04/04)

Sonochemically enhanced Wurtz coupling using lithium metal has been investigated for a number of isomeric alkyl bromides under a variety conditions. The products result from direct coupling of short lived radicals formed at the metal surface rather than the secondary radicals which can be formed during coupling of aromatic halides and thus give rise to a single major product. Coupling has been extended to dibrominated aryl and alkyl compounds as well as showing that aryl-alkyl coupling is possible. Dibrominated alkyls were found to give low molecular weight oligomers although no reaction occurred for 1,2-isomers. The growth of oligomers in THF may be solubility limited. A simple model is proposed to explain these findings.

New homo-coupling reaction of alkyl, aryl, vinyl, and allyl grignard reagents using trifluoromethanesulfonic anhydride

Nishiyama, Tomihiro,Seshita, Takeshi,Shodai, Hiroshi,Aoki, Kazushige,Kameyama, Hideaki,Komura, Kenichi

, p. 549 - 550 (2007/10/03)

Homo-coupling reaction of various alkyl, aryl, vinyl, and allyl Grignard reagents with trifluoromethanesulfonic anhydride provides a simple and straightforward method for the syntheses of symmetrical carbon-carbon coupling products under mild conditions and in moderate to good yields.

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