7062-12-6

Basic information

• Product Name: 2-cyclohexylidenepropanal
• Synonyms: 2-Cyclohexylidenepropanal; Propanal, 2-cyclohexylidene-
• CAS NO: 7062-12-6
• Molecular Formula: C₉H₁₄O
• Molecular Weight: 138.2069
• Mol File: 7062-12-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 225.1°C at 760 mmHg
• Flash Point: 106.8°C
• Density: 0.948g/cm³
• Vapor Pressure: 0.0879mmHg at 25°C
• Refractive Index: 1.479
• CAS DataBase Reference: 2-cyclohexylidenepropanal(CAS DataBase Reference)
• NIST Chemistry Reference: 2-cyclohexylidenepropanal(7062-12-6)
• EPA Substance Registry System: 2-cyclohexylidenepropanal(7062-12-6)

Safety Data

• Hazardous Substances Data: 7062-12-6(Hazardous Substances Data)

Upstream product

• 58707-01-0 tert-Butyl-[2-trimethylsilanyl-prop-(E)-ylidene]-amine 
• 108-94-1 cyclohexanone 
• 19860-43-6 1-Cyclohexylamino-propen-⁽¹⁾-yl-⁽²⁾-phosphonsaeurediethylester 
• 2622-21-1 1-vinylcyclohexene 
• 201230-82-2 carbon monoxide 
• 3908-31-4 1-Isopropenyl-1-cyclohexanol 
• 1670-47-9 1,1-diethoxycyclohexane 
• 63963-01-9 ethyl 2-cyclohexilidenepropionate 
• 88444-72-8 2-cyclohexylidene-1-propanol 
• 7014-71-3 1-Brom-2-cyclohexyliden-propan 

Downstream Products

• 7071-29-6 4-cyclohexylidenepent-1-en-3-ol 
• 69986-44-3 3-cyclohexylidene-2-butanol 
• 264879-09-6 4-cyclohexylidenepent-1-en-3-one 
• 264879-08-5 4-cyclohexylidene-2-methylpent-1-en-3-one 
• 7071-37-6 4-Oxo-2-cyclohexyliden-penten-⁽³⁾ 
• 7071-32-1 2-Cyclohexyliden-5-brom-penten-3 
• 79405-39-3 <(3-cyclohexylidene-2-butyl)oxy>trimethylsilane 
• 79405-34-8 <<2-(1-methylcyclohexyl)-1-propenyl>oxy>trimethylsilane 

Relevant articles and documents

Nazarov cyclization of 4-cycloalkylidene-5-(trimethylsilyl)pent-1-en-3-one derivatives. Synthesis of spiro[4.5]decane, Spiro[4.4]nonane, and Their derivatives

Spiro[4.5]decane and spiro[4.4]nonane ring systems were synthesized by FeCl3-induced Nazarov cyclization of α-(trimethylsilylmethyl)divinyl ketone derivatives. It was found that the double bond position of the product is controlled by the presence/absence of α'-substituent, while trimethylsilyl group is essential to obtain the products in good yields. Spiro[4.4]nonanes having exo-methylene group underwent rearrangement to bicyclo[4.3.0]nonanes. (C) 2000 Elsevier Science Ltd.

Synthesis of δ-cyclohexyl- and δ,δ-alkylene-α,α-dicarbonyl-substituted dienes and study of their valence isomerization

β-Cycloacrolein, β-cyclohexylmethacrolein, or α-cycloalkylidenalkanals were condensed with methyl acetoacetate or dimethyl malonate to give the δ-cyclohexyl- and δ,δ-alkylene-substituted α,α-dicarbonyl-containing α,β:γ,δ-dienes.The structures of the react