57181-82-5

Basic information

• Product Name: Benzene, (1-bromo-2-methylpropyl)-
• CAS NO: 57181-82-5
• Molecular Formula: C10H13Br
• Molecular Weight: 213.117
• Mol File: 57181-82-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzene, (1-bromo-2-methylpropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (1-bromo-2-methylpropyl)-(57181-82-5)
• EPA Substance Registry System: Benzene, (1-bromo-2-methylpropyl)-(57181-82-5)

Safety Data

• Hazardous Substances Data: 57181-82-5(Hazardous Substances Data)

Upstream product

• 3145-76-4 (2-methylcyclopropyl)benzene 
• 611-69-8 rac-2-methyl-1-phenylpropan-1-ol 
• 100-52-7 benzaldehyde 
• 538-93-2 1-phenyl-2-methylpropane 
• 10035-10-6 hydrogen bromide 

Downstream Products

• 768-49-0 (2-methyl-1-propenyl)-benzene 
• 132625-40-2 1-(2-methyl-1-phenyl-1-propyl)cycloheptapyrrol-2(1H)-one 
• 132625-43-5 2-(2-Methyl-1-phenyl-propoxy)-cyclohepta[b]pyrrole 
• 110047-87-5 meso-2,5-Dimethyl-3,4-diphenylhexan 
• 41283-72-1 ibuprofen ethyl ester 
• 1333501-16-8 2,2,6,6-tetramethyl-1-(2-methyl-1-phenylpropoxy)piperidine 
• 1333501-34-0 2,2,6,6-tetramethyl-1-(2-methyl-1-phenylpropoxy)piperidine-4-ol 
• 1333501-37-3 4-allyloxy-2,2,6,6-tetramethyl-1-(2-methyl-1-phenylpropoxy)piperidine 
• 58040-60-1 (4-methylpent-1-yne-1,3-diyl)dibenzene 
• 611-70-1 phenyl isopropyl ketone 
• 412271-30-8 N-(4-methoxyphenyl)-N-(2-methyl-1-phenylpropyl)amine 

Relevant articles and documents

Method for synthesizing alkyne through catalytic asymmetric cross coupling (by machine translation)

The invention belongs to the field of, asymmetric synthesis, and discloses a method for catalyzing asymmetric cross- coupling to synthesize: an alkyne, and the L method comprises, the following steps, of A: preparing B a cuprous, salt and C a: ligand; preparing a catalyst; adding a base; reacting the compound with the compound with the compound; and reacting the compound with the compound. Of these, one of them, X is selected from the group consisting of, R halogens. 1 Optionally substituted heteroarylsulfonylcyanamide groups selected from the, group consisting, of optionally substituted, phenyl groups In-flight vehicle, R6 Trialkyl silyl groups or alkyl radicals, R2 Cycloalkyl radicals optionally substituted with an, optionally substituted alkyl, (CH radical2 )n R4 Multi,layer chain, n＝0-10,R saw blade4 A group selected, from, the group consisting of phenyl, alkenyl, aralkynyls, noonyloxy,and, noonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulfonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylsulphonylphenyl disiloxy-radicals. R3 A ligand, selected from hydrogen or any of the functional groups, is selected from the group consisting of, hydrogen and any L other functional group. The method, R disclosed by the, A invention has the, advantages of good catalytic, R ’ effect, wide application range. and high catalytic efficiency, and the, method disclosed by the, invention has the. advantages of good catalytic effect, wide application range and high catalytic efficiency. (by machine translation)

PROCESS FOR PREPARING ARYL KETONE

A process for preparing aryl ketones is disclosed. The process includes photo-oxidizing a compound of formula (V), (VI), (VII) or (VIII): in the presence of an oxidative system comprising at least one bromide compound to form aryl ketones. X1, X2, R1, R2, R3, L1, L2, L3, L4, t, n, m and p have the meanings as described in the specification and claims.

Direct and selective benzylic oxidation of alkylarenes via C-H abstraction using alkali metal bromides

A direct benzylic oxidation of alkylarenes via C-H bond abstraction was developed using alkali metal bromides and oxidants under mild conditions. This reaction proceeded with excellent selectivity by thermal oxidation or photooxidation to provide a broad range of carbonyl compounds containing electron-deficient aryl carbonyl compounds in high yields.