19656-95-2

Basic information

• Product Name: 2-Cyclohexene-1-acetaldehyde
• CAS NO: 19656-95-2
• Molecular Formula: C8H12O
• Molecular Weight: 124.183
• Mol File: 19656-95-2.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexene-1-acetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexene-1-acetaldehyde(19656-95-2)
• EPA Substance Registry System: 2-Cyclohexene-1-acetaldehyde(19656-95-2)

Safety Data

• Hazardous Substances Data: 19656-95-2(Hazardous Substances Data)

Upstream product

• 51284-30-1 3-((Z)-2-Methoxy-vinyl)-cyclohexene 
• 80816-25-7 2-cyclohexenyl vinyl ether 
• 16452-34-9 2-(cyclohex-2-enyl)ethanol 
• 112052-21-8 methyl 2-(cyclohex-2-en-1-yl)acetate 
• 1372709-52-8 C₁₀H₁₇NO₂ 
• 1521-51-3 rac-3-bromocyclohexene 
• 6305-63-1 diethyl 2-(cyclohex-2-enyl)malonate 
• 21331-58-8 ethyl (cyclohexen-3-yl)acetate 
• 110-83-8 cyclohexene 
• 7012-38-6 2-chlorocyclohexyl 2-chloroethyl ether 
• 57433-61-1 2-bromocyclohexyl 2-bromoethyl ether 
• 76644-52-5 rac-3-acetoxycyclohexene 
• 822-67-3 Cyclohex-2-enol 
• 34939-28-1 dimethyl 2-(cyclohex-2-en-1-yl)malonate 

Downstream Products

• 69504-98-9 3-(2-Cyclohexenyl)-1-nitropropan 
• 3675-31-8 2-(cyclohex-2-enyl)acetic acid 
• 17639-69-9 5-(1-methylene-2-cyclohexenyl)hydantoin 
• 221617-23-8 N-[2-(cyclohex-2-enyl)ethyl]-6-iodo-1,3-benzodioxole-5-methanamine 
• 880645-28-3 (2-cyclohex-2-enylethyl)prop-2-ynylamine 
• 63814-03-9 1,2,3,3a,4,5,12b,12c-octahydro-7H-1,3-benzodioxolo[5,6-c]pyrrolo[3,2,1-ij]quinoline 
• 221617-24-9 N-chloro-N-[2-(cyclohex-2-enyl)ethyl]-6-iodo-1,3-benzodioxole-5-methanamine 
• 223484-73-9 N'-(benzo[1,3]dioxole-5-carbonyl)-N'-(2-cyclohex-2-enyl-ethyl)-N-phenyl-hydrazinecarbodithioic acid methyl ester 
• 82700-05-8 2-(cyclohex-2-en-1-yl)acetonitrile 
• 317337-95-4 C₁₀H₁₄N₂ 
• 123729-78-2 N-<2-cyano-3-(cyclohex-2-enyl)propionyl>-N,N'-di-t-butylurea 
• 123729-77-1 (E)-3-(3-nitroallyl)cyclohexene 
• 16562-82-6 β-(cyclohexen-2-yl)alanine 
• 880645-22-7 N-chloro-(2-cyclohex-2-enylethyl)prop-2-ynylamine 

Relevant articles and documents

Highly efficient Narasaka-Heck cyclizations mediated by P(3,5-(CF 3)2C6H3)3: Facile access to N-heterobicyclic scaffolds

N-heterobicyclic scaffolds: Highly efficient palladium-catalyzed cyclizations of oxime esters with cyclic alkenes were used as a general entry to perhydroindole and related scaffolds. The chemistry is reliant upon the use of P(3,5-(CF3)2/

Tandem Pd(II)-catalyzed vinyl ether exchange-claisen rearrangement as a facile approach to γ,δ-unsaturated aldehydes

(Chemical Equation Presented) A sequential allyl vinyl ether formation-Claisen rearrangement process catalyzed by a palladium(II)- phenanthroline complex is reported. The effects of allylic alcohol structure, type of vinylating agent, and palladium catalysts are discussed. This method provides a convenient approach to γ,δ unsaturated aldehydes under mild conditions that avoid the use of toxic Hg(II) catalysts. The new methodology has been successfully demonstrated on the kilogram scale.

4-SUBSTITUTED IMIDAZOLE-2-THIONES AND IMIDAZOL- 2-ONES AS AGONISTS OF THE ALPHA- 2B AND ALPHA-2C ADRENERGIC RECEPTORS

Compounds of Formula (I): where X is S and the variables have the meaning defined in the specification are specific or selective to alpha2B and/or alpha2C adrenergic receptors in preference over alpha2A adrenergic receptors, and as such have no or only minimal cardivascular and/or sedatory activity. These compounds of Formula (I) are useful as medicaments in mammals, including humans, for treatment of diseases and or alleviations of conditions which are responsive to treatment by agonists of alpha2B adrenergic receptors. Compounds of Formula (I) where X is O also have the advantageous property that they have no or only minimal cardivascular and/or sedatory activity and are useful for treating pain and other conditions with no or only minimal cardivascular and/or sedatory activity.