94453-46-0

Basic information

• Product Name: 1-cyclohexylpent-3-en-1-ol
• Synonyms: 1-cyclohexylpent-3-en-1-ol
• CAS NO: 94453-46-0
• Molecular Weight: 168.279
• Mol File: 94453-46-0.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 1-cyclohexylpent-3-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-cyclohexylpent-3-en-1-ol(94453-46-0)
• EPA Substance Registry System: 1-cyclohexylpent-3-en-1-ol(94453-46-0)

Safety Data

• Hazardous Substances Data: 94453-46-0(Hazardous Substances Data)

Upstream product

• 4784-77-4 (E/Z)-crotyl bromide 
• 2043-61-0 cyclohexanecarbaldehyde 
• 75851-67-1 4,4,5,5-tetramethyl-2-(1-methyl-2-propenyl)-1,3,2-dioxaborolane 
• 31197-41-8 crotyltributylstannane 
• 19781-52-3 2,3-dimethylpent-4-en-2-ol 
• 286-45-3 8-oxabicyclo[5.1.0]octane 
• 467245-96-1 2-((E)-But-2-enyl)-4,4,5,5-tetramethyl-2-[((E)-propenyl)oxy]-[1,3,2]dioxasilolane 
• 467245-73-4 2-((E)-But-2-enyl)-4,4,5,5-tetramethyl-2-vinyloxy-[1,3,2]dioxasilolane 
• 467245-75-6 2-((Z)-But-2-enyl)-4,4,5,5-tetramethyl-2-vinyloxy-[1,3,2]dioxasilolane 
• 69611-02-5 (E)-2-(but-2-enyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 66534-32-5 α,α-diisopropyl-β-methylhomoallylic alcohol 
• 4784-77-4 (E)-1-Bromo-2-butene 
• 221676-47-7 1-cyclohexyl-2-methyl-but-3-en-1-ol 

Downstream Products

• 130276-73-2 (4S,6S)-6-Cyclohexyl-4-ethyl-2,2-dimethyl-[1,2]oxasilinane 
• 130276-79-8 (1S,3S)-1-Cyclohexyl-3-ethyl-butane-1,4-diol 
• 130276-77-6 Bromomethyl-((Z)-(S)-1-cyclohexyl-pent-3-enyloxy)-dimethyl-silane 

Relevant articles and documents

Development of a highly α-regioselective indium-mediated allylation reaction in water

Linear α homoallylic alcohol adducts were obtained with high regioselectivities in moderate to good yields using allylic indium reagents in the presence of 10 M water. The exceptionally high regioselectivities observed were neither steric nor electronic i

Highly stereoselective synthesis of z-homoallylic alcohols by kinetic resolution of racemic secondary allyl boronates

α to Z: Racemic α-chiral allyl boronates, which are readily synthesized from the respective primary allyl halides, undergo a highly efficient kinetic resolution in a face- and Z-selective allylation of aldehydes catalyzed by the chiral Bronsted acid (R)-TRIP (see scheme; Epin=tetraethylethylene glycol). Copyright

Epoxide as an aldehyde equivalent in allyl-transfer reaction with γ-adduct of homoallylic alcohol (allyl donor) giving α-adduct of homoallylic alcohol

Acid-catalyzed reactions of epoxides 2 with homoallylic alcohol γ-adducts, 1 [Me2C(OH)CHRCH{double bond, long}CH2], afford homoallylic alcohol α-adducts 3-5 via allyl-transfer reaction, sometimes being more effective than those using