1612-03-9

Basic information

• Product Name: (3-methylbut-1-yn-1-yl)benzene
• Synonyms: (3-Methylbut-1-yn-1-yl)benzene; 1-Phenyl-3-methyl-1-butyne; benzene, (3-methyl-1-butyn-1-yl)-; Benzene, (3-methyl-1-butynyl)-; Isopropyl-phenyl-acetylene
• CAS NO: 1612-03-9
• Molecular Formula: C₁₁H₁₂
• Molecular Weight: 144.213
• Mol File: 1612-03-9.mol
• Article Data: 38

Chemical Properties

• Boiling Point: 215.2°C at 760 mmHg
• Flash Point: 80.1°C
• Density: 0.92g/cm³
• Vapor Pressure: 0.219mmHg at 25°C
• Refractive Index: 1.525
• CAS DataBase Reference: (3-methylbut-1-yn-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (3-methylbut-1-yn-1-yl)benzene(1612-03-9)
• EPA Substance Registry System: (3-methylbut-1-yn-1-yl)benzene(1612-03-9)

Safety Data

• Hazardous Substances Data: 1612-03-9(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 109431-70-1 4-phenylbut-3-yn-2-yl acetate 
• 628-71-7 1-Heptyne 
• 1776-66-5 triisopropylborane 
• 5324-64-1 2-(benzenesulfonyl)ethynylbenzene 
• 1539-32-8 4-isopropyl-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester 
• 1483-82-5 phenylethynyl chloride 
• 13291-18-4 isopropenylmagnesium bromide 
• 75-29-6 isopropyl chloride 
• 1191-99-7 2,3-dihydro-2H-furan 
• 875-79-6 1,2-dimethylindole 
• 61423-02-7 ethyl 1,1-dimethyl-3-phenylpropargyl acetate 
• 920-39-8 isopropylmagnesium bromide 
• 637-44-5 phenylpropyolic acid 

Downstream Products

• 1719-19-3 2-Methyl-4-phenyl-3-butyn-2-ol 
• 611-69-8 rac-2-methyl-1-phenylpropan-1-ol 
• 705-58-8 3-methyl-1-phenyl-2-butanol 
• 36004-04-3 ethyl (E)-1-phenylbut-1-en-3-ol 
• 103-05-9 4-phenyl-2-methyl-2-butanol 
• 57132-28-2 (E)-2-methyl-4-phenylbut-3-en-2-ol 
• 100-51-6 benzyl alcohol 
• 1283231-63-9 (Z)-4,4,5,5-tetramethyl-2-(3-methyl-1-phenylbut-1-en-2-yl)-1,3,2-dioxaborolane 
• 849667-47-6 (2-isopropyl-3-phenyl-cycloprop-2-enyl)-methanol 
• 849667-50-1 2-isopropyl-3-phenyl-cycloprop-2-enecarbaldehyde 
• 582-62-7 3-methyl-1-phenylbutan-1-one 
• 2893-05-2 3-methyl-1-phenylbutan-2-one 

Relevant articles and documents

Enantioselective Three-Component Coupling of Heteroarenes, Cycloalkenes and Propargylic Acetates

Asymmetric coupling proceeds efficiently between propargylic acetates, cycloalkenes and electron-rich heteroarenes including indoles, pyrroles, activated furans and thiophenes. 2,3-Disubstituted tetrahydrofurans and pyrrolidines are produced in trans conf

An Enzymatic Platform for Primary Amination of 1-Aryl-2-alkyl Alkynes

Propargyl amines are versatile synthetic intermediates with numerous applications in the pharmaceutical industry. An attractive strategy for efficient preparation of these compounds is nitrene propargylic C(sp3)-H insertion. However, achieving this reacti

Nickel-Catalyzed Sonogashira Coupling Reactions of Nonactivated Alkyl Chlorides under Mild Conditions

The two nickel chlorides1and2with [P,S] and [P,Se] bidentate ligands, respectively, were synthesized and used as catalysts for Sonogashira coupling reaction. Both1and2are efficient catalysts for Sonogashira C(sp3)-C(sp) coupling reactions. Comp