36872-03-4

Basic information

• Product Name: (2E)-(3,3-dimethylcyclohexylidene)ethanal
• Synonyms: (3,3-DIMETHYLCYCLOHEXYLIDENE)ACETALDEHYDE; (E)-(3,3-Dimethylcyclohexylidene)acetaldehyde; Acetaldehyde, (3,3-dimethylcyclohexylidene)-, (2E)-; Acetaldehyde, (3,3-dimethylcyclohexylidene)-, (E)-; cis-3,3-Dimethylcyclohexylideneethanal; trans-3,3-Dimethylcyclohexylideneethanal
• CAS NO: 36872-03-4
• Molecular Formula: C₁₀H₁₆O
• Molecular Weight: 152.2334
• Mol File: 36872-03-4.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 226.6°C at 760 mmHg
• Flash Point: 95.6°C
• Density: 0.955g/cm³
• Vapor Pressure: 0.081mmHg at 25°C
• Refractive Index: 1.514
• CAS DataBase Reference: (2E)-(3,3-dimethylcyclohexylidene)ethanal(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-(3,3-dimethylcyclohexylidene)ethanal(36872-03-4)
• EPA Substance Registry System: (2E)-(3,3-dimethylcyclohexylidene)ethanal(36872-03-4)

Safety Data

• Hazardous Substances Data: 36872-03-4(Hazardous Substances Data)

Upstream product

• 30346-27-1 (E)-2-(3,3-Dimethylcyclohexylidene)ethanol 
• 78424-79-0 (5-methyl-3-methyleneoct-6-en-1-yl)(phenyl)sulfane 
• 26532-23-0 (Z)-3,3-Dimethylcyclohexane-Δ^1,β-ethanol 
• 30346-23-7 3,3-Dimethyl-Z-cyclohexylidenessigsaeuremethylester 
• 57559-99-6 Acetic acid 1-ethynyl-3,3-dimethyl-cyclohexyl ester 
• 82528-50-5 C₁₇H₂₄N₂O₃S 
• 82528-41-4 (EZ)-6-oxo-2-ochtoden-1-yl trifluoroacetate 
• 82528-38-9 1-acetoxy-6-phenylthio-2-ochtodene 
• 82528-40-3 (EZ)-6-hydroxy-2-ochtoden-1-yl trifluoroacetate 
• 82528-39-0 6-phenylthio-2-ochtoden-1-ol 
• 82528-37-8 1-chloro-6-phenylthio-2-ochtodene 
• 70473-42-6 [1-(1-Chloro-1-methyl-ethyl)-4-methylene-hex-5-enylsulfanyl]-benzene 
• 82528-42-5 (EZ)-1-hydroxy-2-ochtoden-6-one 
• 123-35-3 7-methyl-3-methene-1,6-octadiene 

Relevant articles and documents

Tandem Michael - Wittig - Horner reaction: One-pot synthesis of δ- substituted α,β-unsaturated carboxylic acid derivatives - application to a concise synthesis of (Z)- and (E)-ochtoden-1-al

A new tandem Michael-Wittig-Horner reaction has been developed to produce in high yields δ-substituted α,β-unsaturated esters, amides and lactones. The reaction has been successfully applied to a concise synthesis of (E)- and (Z)-ochtoden-1-als, component

THE STEREOSPECIFIC FORMATION OF AN EXOCYCLIC ALKENE BY A CONSECUTIVE RADICAL CYCLIZATION-ELEIMINATION

The iodovinylstannanes 4 and 5 were prepared by the conjugate addition of the tri-n-butyltin moiety to a substituted propiolic ester.Compounds 4 and 5 underwent a radical cyclization-elimination reaction to stereospecifically generate an exocyclic alkene.

New Synthetic Methods for γ-Geraniol, Boll Weevil Pheromone, and α-Damascone Employing 2-(Hydroxymethyl)-4-(phenylthio)-1-butene as a Building Block

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