56963-36-1

Basic information

• Product Name: 4-Hexen-1-yn-3-ol, 1-phenyl-
• CAS NO: 56963-36-1
• Molecular Formula: C12H12O
• Molecular Weight: 172.227
• Mol File: 56963-36-1.mol

Chemical Properties

• CAS DataBase Reference: 4-Hexen-1-yn-3-ol, 1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Hexen-1-yn-3-ol, 1-phenyl-(56963-36-1)
• EPA Substance Registry System: 4-Hexen-1-yn-3-ol, 1-phenyl-(56963-36-1)

Safety Data

• Hazardous Substances Data: 56963-36-1(Hazardous Substances Data)

Upstream product

• 6738-06-3 phenylethynylmagnesium bromide 
• 123-73-9 crotonaldehyde 
• 536-74-3 phenylacetylene 
• 591-50-4 iodobenzene 
• 59095-52-2 hex-4-en-1-yn-3-ol 

Downstream Products

• 1263383-64-7 C₂₇H₃₅O₇P 
• 1263383-63-6 C₂₅H₃₁O₇P 
• 109918-90-3 (E)-3-Hydroperoxy-1-phenyl-hex-4-en-1-yn-3-ol 
• 100123-13-5 6-phenyl-hexa-1,3-dien-5-yne 
• 637-44-5 phenylpropyolic acid 
• 1019-57-4 acetaldehyde 2,4-dinitrophenylhydrazine 
• 725-00-8 propanal 2,4-dinitrophenyl hydrazone 
• 1527-96-4 crotonaldehyde (2,4-dinitrophenyl)hydrazone 
• 109918-92-5 1-phenyl-4,5-epoxy-1-hexyn-3-one 
• 16121-40-7 1-phenyl-4-hexen-1-yn-3-one 
• 29582-53-4 trans-3-Methyl-7-phenylhept-4-en-6-inal 
• 29582-52-3 (Z)-3-methyl-7-(phenyl)hept-4-en-6-ynal 

Relevant articles and documents

Convenient synthesis of polysubstituted 3-iodofurans through the tandem ring-opening/cyclization reaction of 1-alkynyl-2,3-epoxy alcohols

A novel method for the synthesis of highly substituted iodine-containing furans has been developed by the cyclization of 1-(arylethynyl)-2,3-epoxy alcohols (1-aryl-4,5-epoxyalk-1-yn-3-ols) with alcohols as nucleophiles under very mild reaction conditions.

AUTOOXIDATION OF ACETYLENES AND THEIR DERIVATIVES. XXV. 1-PHENYL-4-PENTEN-1-YN-3-0L AND 1-PHENYL-4-HEXEN-1-YN-3-OL

During the autooxidation of secondary enynyl alcohols attack by oxygen takes place at the C-H bonds at the α position to the triple and double bonds and the hydroxyl group.The initially formed unstable hydroxyhydroperoxides dissociate under the oxidation conditions into the corresponding enynyl ketones, acetylenic keto epoxydes, and products from degradation of the carbon skeleton.