1985-57-5 Usage
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.
Used in Coatings Industry:
(1,1-dimethylbutyl)benzene is used as a solvent for [application reason] in the coatings industry, helping to dissolve and apply coatings effectively.
Used in Adhesives Industry:
(1,1-dimethylbutyl)benzene is used as a solvent for [application reason] in the adhesives industry, aiding in the proper application and bonding of adhesives.
Used in Industrial Cleaning Products:
(1,1-dimethylbutyl)benzene is used as a solvent for [application reason] in industrial cleaning products, assisting in the removal of dirt, grease, and other contaminants.
Used as a Chemical Intermediate:
(1,1-dimethylbutyl)benzene is used as a chemical intermediate for [application reason] in the production of other compounds, contributing to the synthesis of various chemical products.
Note: The specific "application reasons" are not provided in the materials, so they are left as placeholders to be filled in with the actual reasons based on the specific properties and benefits of (1,1-dimethylbutyl)benzene in each application.
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
1985-57-5Relevant 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.
