2051-99-2

Basic information

• Product Name: 1-BROMO-4-ISOBUTYLBENZENE
• Synonyms: 4-BROMOISOBUTYLBENZENE;1-BROMO-4-ISOBUTYLBENZENE;P-BROMO-ISO-BUTYLBENZENE;P-BROMISOBUTYLBENZENE;benzene,1-(2-methylpropyl)-4-bromo-;1-Isobutyl-4-bromobenzene;1-Bromo-4-(2-methylpropyl)benzene;1-Bromo-4-(2-methylprop-1-yl)benzene, 1-(4-Bromophenyl)-2-methylpropane
• CAS NO: 2051-99-2
• Molecular Formula: C₁₀H₁₃Br
• Molecular Weight: 213.11
• Product Categories: Starting Raw Materials & Intermediates
• Mol File: 2051-99-2.mol
• Article Data: 7

Chemical Properties

• Melting Point: -49.68 °C
• Boiling Point: 236.986 °C at 760 mmHg
• Flash Point: 96.587 °C
• Appearance: /
• Density: 1.24 g/cm³
• Vapor Pressure: 0.0706mmHg at 25°C
• Refractive Index: 1.525
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1-BROMO-4-ISOBUTYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-4-ISOBUTYLBENZENE(2051-99-2)
• EPA Substance Registry System: 1-BROMO-4-ISOBUTYLBENZENE(2051-99-2)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 2051-99-2(Hazardous Substances Data)

Usage

General Description

1-Bromo-4-isobutylbenzene is a chemical compound with the molecular formula C10H13Br. It is a colorless to light yellow liquid that is insoluble in water, but soluble in organic solvents. It is used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It can also be used as a reagent in organic synthesis. The compound is a halogenated aromatic hydrocarbon, and as such, it is important to handle it with caution due to its potential hazards as a chemical irritant and environmental contaminant. However, it is a valuable compound in the field of organic chemistry due to its versatility and reactivity in various chemical reactions.

InChI:InChI=1/C10H13Br/c1-8(2)7-9-3-5-10(11)6-4-9/h3-6,8H,7H2,1-2H3

Upstream product

• 538-93-2 1-phenyl-2-methylpropane 
• 1122-91-4 4-bromo-benzaldehyde 
• 49660-93-7 4'-bromoisobutyrophenone 
• 75-30-9 2-iodo-propane 
• 57477-93-7 hydrazone of p-bromobenzaldehyde 
• 6731-23-3 triisobutylindium 
• 130447-21-1 (4-bromophenyl)zinc(II) chloride 
• 106-37-6 1.4-dibromobenzene 
• 18620-02-5 (4-bromophenyl)magnesium bromide 
• 56985-68-3 1-bromo-4-(2-methyl-1-propenyl)benzene 
• 56985-67-2 4-Bromo-α-(1-methylethyl)benzenemethanol 
• 83558-89-8 2-methyl-3-(4-bromophenyl)-propene 

Downstream Products

• 19409-00-8 3-(p-Isobutyl-phenyl)-2-hydroxy-propylchlorid 
• 1001010-49-6 5-(4-isobutyl-phenyl)-furan-2-carbaldehyde 
• 81576-55-8 (S)-(+)-methyl 2-(4-isobutylphenyl)propionate 
• 81576-57-0 (R)-ibuprofen methyl ester 
• 64622-17-9 propan-2-yl 2-[4-(2-methylpropyl)phenyl]propanoate 
• 64622-17-9 (R)-ibuprofen isopropyl ester 
• 1352037-33-2 benzyl 2-[4-(2-methylpropyl)phenyl]propanoate 

Relevant articles and documents

Method for preparing para-substituted bromobenzene

The present application relates to a method for preparing para-substituted bromobenzene represented by formula 2, which is characterized in that the method comprises the steps of: in organic solvents,in the presence of alkali, the compound represented by

Nickel-Catalyzed Cross-Coupling of Umpolung Carbonyls and Alkyl Halides

An effective nickel-catalyzed cross-coupling of Umpolung carbonyls and alkyl halides was developed. Complementary to classical alkylation techniques, this reaction utilizes Umpolung carbonyls as the environmentally benign alkyl nucleophiles, providing an efficient and selective catalytic alternative to the traditional use of highly reactive alkyl organometallic reagents.

Highly selective palladium-catalyzed oxidative Csp2-Csp 3 cross-coupling of arylzinc and alkylindium reagents through double transmetallation

Using desyl chloride (2-chloro-1,2-diphenylethanone) as the oxidant, the palladium-catalyzed reaction of arylzinc with alkylindium reagents occurred smoothly in a highly selective manner to afford the products in 57-90% yields. Preliminary kinetic data in