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594-82-1 Usage

Description

2,2,3,3-Tetramethylbutane is a hydrocarbon and one of the isomers of octane. Octanes may be found in gasoline.

Synthesis Reference(s)

The Journal of Organic Chemistry, 21, p. 322, 1956 DOI: 10.1021/jo01109a016

Check Digit Verification of cas no

The CAS Registry Mumber 594-82-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 594-82:
(5*5)+(4*9)+(3*4)+(2*8)+(1*2)=91
91 % 10 = 1
So 594-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H18/c1-7(2,3)8(4,5)6/h1-6H3

594-82-1 Well-known Company Product Price

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  • Aldrich

  • (540846)  2,2,3,3-Tetramethylbutane  ≥94%

  • 594-82-1

  • 540846-1G

  • 790.92CNY

  • Detail

594-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3-TETRAMETHYLBUTANE

1.2 Other means of identification

Product number -
Other names 2,2,4,4-tetramethylbutane

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:594-82-1 SDS

594-82-1Relevant articles and documents

Foster,Hickinbottom

, p. 215,217 (1960)

Oxidative coupling reactions of grignard reagents with nitrous oxide

Kiefer, Gregor,Jeanbourquin, Loic,Severin, Kay

supporting information, p. 6302 - 6305 (2013/07/19)

Catalysis with laughing gas: N2O in combination with transition-metal catalysts allow the oxidative homo- and cross-coupling of Grignard reagents. The reactions can be performed under mild conditions despite the inert character of N2O. Copyright

Silver-catalyzed carbomagnesiation of terminal aryl and silyl alkynes and enynes in the presence of 1,2-dibromoethane

Fujii, Yuuki,Terao, Jun,Kambe, Nobuaki

scheme or table, p. 1115 - 1117 (2009/07/10)

Regioselective carbomagnesiation of terminal alkynes and enynes with alkyl Grignard reagents has been achieved by the combined use of a silver catalyst and 1,2-dibromoethane. The Royal Society of Chemistry 2009.

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