5436-42-0

Basic information

• Product Name: 4-methoxy-2-methyl-1-(propan-2-yl)benzene
• CAS NO: 5436-42-0
• Molecular Formula: C₁₁H₁₆O
• Molecular Weight: 164.2441
• Mol File: 5436-42-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 231.4°C at 760 mmHg
• Flash Point: 82.9°C
• Density: 0.913g/cm³
• Vapor Pressure: 0.0947mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: 4-methoxy-2-methyl-1-(propan-2-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-2-methyl-1-(propan-2-yl)benzene(5436-42-0)
• EPA Substance Registry System: 4-methoxy-2-methyl-1-(propan-2-yl)benzene(5436-42-0)

Safety Data

• Hazardous Substances Data: 5436-42-0(Hazardous Substances Data)

Upstream product

• 24826-73-1 4-isopropenyl-3-methyl-anisole 
• 148706-30-3 2-methyl-4-methoxyphenylmagnesium bromide 
• 91968-30-8 2-(4-methoxy-2-methyl-phenyl)-propan-2-ol 
• 88739-11-1 1-Isopropyl-4-methoxy-2-methyl-cyclohexa-1,4-diene 
• 3228-02-2 3-Methyl-4-isopropylphenol 
• 77-78-1 dimethyl sulfate 
• 74-83-9 methyl bromide 

Downstream Products

• 102589-89-9 3,5'-diisopropyl-6,4'-dimethoxy-2,2'-dimethyl-benzophenone 
• 132778-00-8 1-(3-isopropyl-6-methoxy-2-methyl-phenyl)-ethanone 
• 105337-35-7 1-<6-hydroxy-2-methyl-3-(1-methylethyl)phenyl>-ethanone 
• 105337-86-8 3-isopropyl-6-methoxy-2-methyl-benzaldehyde 
• 88739-11-1 1-Isopropyl-4-methoxy-2-methyl-cyclohexa-1,4-diene 
• 64854-00-8 4-isopropyl-3-methylcyclohex-3-enone 
• 23053-85-2 6-hydroxy-3-isopropyl-2-methyl-benzoic acid 
• 110049-23-5 3-isopropyl-6,4'-dimethoxy-2-methyl-benzophenone 
• 109250-50-2 4'-hydroxy-3-isopropyl-6-methoxy-2-methyl-benzophenone 
• 23053-74-9 2-Chloracetyl-p-thymol 
• 24826-71-9 3-Methyl-4-isopropyl-2-cyclohexen-1-one 
• 102162-06-1 3-isopropyl-6-methoxy-2-methyl-deoxybenzoin 
• 102020-37-1 1-(3-isopropyl-6-methoxy-2-methyl-phenyl)-octan-1-one 
• 107151-01-9 2-chloro-1-(3-isopropyl-6-methoxy-2-methyl-phenyl)-ethanone 

Relevant articles and documents

Total Syntheses of Crinipellins Enabled by Cobalt-Mediated and Palladium-Catalyzed Intramolecular Pauson–Khand Reactions

Efficient total syntheses of the naturally occurring, potent antibiotic compounds (?)-crinipellin A and (?)-crinipellin B are described. The key advanced intermediate, a fully functionalized tetraquinane core, was constructed by a novel thiourea/palladium-catalyzed Pauson–Khand reaction. This intermediate can serve as a common intermediate for the collective total synthesis of other members of the crinipellin family.