130955-17-8

Basic information

• Product Name: 4-(2-BROMOPHENYL)-2-METHYL-1-BUTENE 97
• Synonyms: 4-(2-BROMOPHENYL)-2-METHYL-1-BUTENE 97
• CAS NO: 130955-17-8
• Molecular Formula: C₁₁H₁₃Br
• Molecular Weight: 225.128
• Mol File: 130955-17-8.mol

Chemical Properties

• Boiling Point: 253.7°Cat760mmHg
• Flash Point: 222 °F
• Appearance: /
• Density: 1.215 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0287mmHg at 25°C
• Refractive Index: n20/D 1.5430(lit.)
• CAS DataBase Reference: 4-(2-BROMOPHENYL)-2-METHYL-1-BUTENE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-BROMOPHENYL)-2-METHYL-1-BUTENE 97(130955-17-8)
• EPA Substance Registry System: 4-(2-BROMOPHENYL)-2-METHYL-1-BUTENE 97(130955-17-8)

Safety Data

• Hazard Codes: N
• Statements: 50/53
• Safety Statements: 60-61
• RIDADR: UN 3077 9/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 130955-17-8(Hazardous Substances Data)

Usage

Molecular Weight

207.1 g/mol

Physical State

Clear, colorless liquid

Purity Level

97%

Family

Alkene compounds

Uses

Synthesis of pharmaceuticals
Synthesis of agrochemicals
Production of organic compounds
Chemical intermediate in dye production
Chemical intermediate in perfume production
Chemical intermediate in flavor production

InChI:InChI=1/C11H13Br/c1-9(2)7-8-10-5-3-4-6-11(10)12/h3-6H,1,7-8H2,2H3

Upstream product

• 33324-92-4 (2-methylallyl)magnesium bromide 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 5674-01-1 2-methylallylmagnesium chloride 

Downstream Products

• 121134-54-1 1-iodo-2-(3-methylbut-3-en-1-yl)benzene 
• 1101859-09-9 2-(3-methylbut-3-enyl)benzaldehyde 
• 6683-51-8 2-methyl-4-phenyl-1-butene 
• 4912-92-9 1,1-dimethylindan 
• 2717-44-4 2-methyl-3,4-dihydronaphthalene 
• 732249-06-8 2-(3-methylbut-3-en-1-yl)benzoic acid 
• 1571984-67-2 9-[2-(3-methyl-3-buten-1-yl)phenyl]-9-borabicyclo[3.3.1]nonane 
• 1092491-43-4 C₁₁H₁₅BrO 

Relevant articles and documents

Iridium(I)-Catalyzed Intramolecular Hydrocarbonation of Alkenes: Efficient Access to Cyclic Systems Bearing Quaternary Stereocenters

A catalytic, versatile and atom-economical C?H functionalization process that provides a wide variety of cyclic systems featuring methyl-substituted quaternary stereocenters is described. The method relies on the use of a cationic IrI–bisphosph

Copper-Catalyzed Amino Lactonization and Amino Oxygenation of Alkenes Using O-Benzoylhydroxylamines

A copper-catalyzed amino lactonization of unsaturated carboxylic acids has been achieved as well as the analogous intermolecular three-component amino oxygenation of olefins. The transformation features mild conditions and a remarkably broad substrate sco

Synthesis of indolines via a domino Cu-catalyzed amidation/cyclization reaction

(Chemical Equation Presented) A highly efficient one-pot procedure for the synthesis of indolines and their homologues based on a domino Cu-catalyzed amidation/nucleophilic substitution reaction has been developed. Substituted 2-iodophenethyl mesylates and related compounds afforded the corresponding products in excellent yields. No erosion of optical purity was observed when transforming enantiomerically pure mesylates under the reaction conditions.