943621-73-6

Basic information

• Product Name: 4-phenylbutane-1,2,4-triol
• Synonyms: 4-phenylbutane-1,2,4-triol
• CAS NO: 943621-73-6
• Molecular Weight: 182.219
• Mol File: 943621-73-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-phenylbutane-1,2,4-triol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenylbutane-1,2,4-triol(943621-73-6)
• EPA Substance Registry System: 4-phenylbutane-1,2,4-triol(943621-73-6)

Safety Data

• Hazardous Substances Data: 943621-73-6(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 61276-54-8 2-(oxiran-2-yl)-1-phenylethan-1-ol 
• 80735-94-0 1-Phenyl-3-buten-1-ol 

Downstream Products

• 948050-79-1 1-phenylhex-5-ene-1,3-diol 
• 140854-63-3 (+/-)-(1S,3R)-1-phenylhex-5-en-1,3-diol 
• 140854-62-2 (+/-)-(1S,3S)-1-phenylhex-5-en-1,3-diol 
• 39850-43-6 (+/-)-3-hydroxy-3-phenyl-propionaldehyde 

Relevant articles and documents

Green Organocatalytic Dihydroxylation of Alkenes

An inexpensive, green, metal-free one-pot procedure for the dihydroxylation of alkenes is described. H2O2 and 2,2,2-trifluoroacetophenone were employed as the oxidant and organocatalyst, respectively, in this highly sustainable protocol in which a variety of homoallylic alcohols, aminoalkenes, and simple alkenes were converted into the corresponding polyalcohols in good to excellent yields. This process takes advantage of an epoxidation reaction followed by an acidic treatment in which water participates in the ring opening of the in situ prepared epoxide to lead to the desired product.

Gold-catalyzed cycloisomerizations of ene-ynamides

The gold-catalyzed cycloisomerizations of 1,6-ene-ynamides proceed under mild conditions and lead to cyclobutanones from terminal or trimethylsilyl substituted ynamides, or to carbonyl compounds bearing a 2,3-methanopyrrolidine subunit from substrates pos