128894-19-9

Basic information

• Product Name: Benzene, [(E)-2-cyclohexen-1-ylidenemethyl]-
• CAS NO: 128894-19-9
• Molecular Formula: C13H14
• Molecular Weight: 170.254
• Mol File: 128894-19-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, [(E)-2-cyclohexen-1-ylidenemethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(E)-2-cyclohexen-1-ylidenemethyl]-(128894-19-9)
• EPA Substance Registry System: Benzene, [(E)-2-cyclohexen-1-ylidenemethyl]-(128894-19-9)

Safety Data

• Hazardous Substances Data: 128894-19-9(Hazardous Substances Data)

Upstream product

• 34492-42-7 2-hydroxybenzylidenecyclohexane 
• 4714-50-5 7-benzoyl-7-aza-bicyclo[4.1.0]heptane 
• 100-52-7 benzaldehyde 
• 68820-12-2 cyclohexyl-N-tosyl aziridine 
• 108-94-1 cyclohexanone 
• 286-20-4 cyclohexane-1,2-epoxide 
• 136559-08-5 6-Benzyl-2-cyclohexen-1-ol 
• 83845-68-5 trans-2-<1-(Phenylseleno)benzyl>cyclohexanol 
• 930-66-5 1-chlorocyclohexene 

Downstream Products

• 141191-74-4 trans-4-Benzylcyclohexan-1-ol 
• 141191-75-5 cis-4-Benzylcyclohexan-1-ol 

Relevant articles and documents

Formation of P-Ylide under Neutral and Metal-Free Conditions: Transformation of Aziridines and Epoxides to Conjugated Dienes in the Presence of Phosphine

A general approach to formation of the P-ylide from the reaction of aziridines or epoxides with organophosphine under neutral and metal-free conditions is realized. Conjugated diene derivatives based on this kind of P-ylide were prepared in a facile and c

Rearrangement of allylic and propargylic alcohols catalyzed by the combined use of tetrabutylammonium perrhenate(VII) and p-toluenesulfonic acid

Allylic rearrangement and/or dehydration reaction of allylic alcohols proceeds smoothly by the use of catalytic amounts of tetrabutylammonium perrhenate and p-toluenesulfonic acid hydrate. Treatment of propargylic alcohols with the catalysts at room temperature affords the rearranged products, α,β-unsaturated carbonyl compounds, while β,γ-unsaturated ketones are obtained as main products by the reaction in refluxing 1,2-dichloroethane. The application of this catalytic system is also described for the preparation of some synthetic intermediates.