103618-34-4

Basic information

• Product Name: (+)-(1S,6S)-6-vinyl-3-cyclohexene-1-carbaldehyde
• Synonyms: (+)-(1S,6S)-6-vinyl-3-cyclohexene-1-carbaldehyde
• CAS NO: 103618-34-4
• Molecular Weight: 136.194
• Mol File: 103618-34-4.mol

Chemical Properties

• CAS DataBase Reference: (+)-(1S,6S)-6-vinyl-3-cyclohexene-1-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(1S,6S)-6-vinyl-3-cyclohexene-1-carbaldehyde(103618-34-4)
• EPA Substance Registry System: (+)-(1S,6S)-6-vinyl-3-cyclohexene-1-carbaldehyde(103618-34-4)

Safety Data

• Hazardous Substances Data: 103618-34-4(Hazardous Substances Data)

Upstream product

• 56799-24-7 trans-6-Vinyl-3-cyclohexen-1-methanol 
• 13149-04-7 (rac)-trans-4,5-bis(hydroxymethyl)cyclohex-1-ene 
• 17673-68-6 dimethyl trans-cyclohex-4-ene-1,2-dicarboxylate 
• 56799-24-7 (4R*,5R*)-4-hydroxymethyl-5-vinylcyclohexene 
• 439919-46-7 cis-1,6-dihydroxymethyl-3-cyclohexene 
• 935-79-5 cis-1,2,3,6-tetrahydrophthalic anhydride 
• 56799-24-7 (-)-(1S,6S)-6-vinyl-3-cyclohexene-1-methanol 
• 4841-84-3 dimethyl cis-1,2,3,6-tetrahydrophthalate 
• 88586-06-5 (3aS,7aR)-3a,4,7,7a-tetrahydroisobenzofuran-1(3H)-one 
• 56799-21-4 cis-6-Hydroxymethyl-3-cyclohexen-1-carbaldehyd 
• 56799-21-4 trans-6-Hydroxy-3-cyclohexen-1-carbaldehyd 
• 31139-02-3 (1R,6S)-6-methoxycarbonyl-3-cyclohexene-1-carboxylic acid 

Downstream Products

• 52811-30-0 trans-4-(cis-1-Propenyl)-5-vinylcyclohexen 
• 52811-30-0 (+/-)-aucantene 
• 52811-30-0 cis-4-(cis-1-Propenyl)-5-vinylcyclohexen 
• 52811-30-0 cis-4-(trans-1-Propenyl)-5-vinylcyclohexen 
• 1123213-62-6 C₁₁H₁₆O 
• 103618-46-8 ((1S,6R)-6-Vinyl-cyclohex-3-enyl)-methanol 

Relevant articles and documents

217. Enantioselective Syntheses and Absolute Configurations of Viridiene and Aucantene, Two Constituents of Algae Pheromone Bouquets

Viridiene ((+)-6; (+)-(3R,4S)-3-((1Z)-1,3-butadienyl)-4-vinylcyclopentene) and aucantene ((+)-18; (+)-(4R,5R)-4-((1E)-1-propenyl)-5-vinylcyclohexene) are constituents of the pheromone bouquets of several brown algae species.Key synthons to the title compo

Studies in iridoid synthesis. Chemoselective transformations of cis-1,2,4,6-tetrahydrophthalic anhydride

In the course of synthetic studies towards the development of diastereoselective routes to secoiridoid aglycones, cis-1,2,4,6- tetrahydrophthalic anhydride was transformed into the corresponding lactone cis-3a,4,7,7a-tetrahydro-3H-isobenzofuran-1-one, whi