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1985-57-5

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1985-57-5 Usage

General Description

(1,1-dimethylbutyl)benzene, also known as diisobutylbenzene, is a chemical compound with the molecular formula C14H20. It is a colorless liquid with a characteristic aromatic odor. It is primarily used as a solvent in various industrial applications, including coatings, adhesives, and industrial cleaning products. It is also used as a chemical intermediate in the production of other compounds. (1,1-dimethylbutyl)benzene is considered to have low toxicity and is not classified as a hazardous substance under most regulations. However, as with any chemical, it is important to handle and store it responsibly to avoid any potential risks to health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 1985-57-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1985-57:
(6*1)+(5*9)+(4*8)+(3*5)+(2*5)+(1*7)=115
115 % 10 = 5
So 1985-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H18/c1-4-10-12(2,3)11-8-6-5-7-9-11/h5-9H,4,10H2,1-3H3

1985-57-5SDS

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 2-methylpentan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1-dimethylbutyl)

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:1985-57-5 SDS

1985-57-5Relevant articles and documents

Catalytic synthesis of n-alkyl arenes through alkyl group cross-metathesis

Dobereiner, Graham E.,Yuan, Jian,Schrock, Richard R.,Goldman, Alan S.,Hackenberg, Jason D.

supporting information, p. 12572 - 12575 (2013/09/23)

n-Alkyl arenes were prepared in a one-pot tandem dehydrogenation/olefin metathesis/hydrogenation sequence directly from alkanes and ethylbenzene. Excellent selectivity was observed when (tBuPCP)IrH2 was paired with tungsten monoaryloxide pyrrolide complexes such as W(NAr)(C 3H6)(pyr)(OHIPT) (1a) [Ar = 2,6-i-Pr2C 6H3; pyr = pyrrolide; OHIPT = 2,6-(2,4,6-i-Pr 3C6H2)2C6H3O]. Complex 1a was also especially active in n-octane self-metathesis, providing the highest product concentrations reported to date. The thermal stability of selected olefin metathesis catalysts allowed elevated temperatures and extended reaction times to be employed.

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