86348-27-8

Basic information

• Product Name: 4-Benzhydryloxy-E-2-buten-1-ol
• Synonyms: 4-Benzhydryloxy-E-2-buten-1-ol
• CAS NO: 86348-27-8
• Molecular Weight: 254.329
• Mol File: 86348-27-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-Benzhydryloxy-E-2-buten-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Benzhydryloxy-E-2-buten-1-ol(86348-27-8)
• EPA Substance Registry System: 4-Benzhydryloxy-E-2-buten-1-ol(86348-27-8)

Safety Data

• Hazardous Substances Data: 86348-27-8(Hazardous Substances Data)

Upstream product

• 776-74-9 Bromodiphenylmethane 
• 128990-33-0 4-Benzhydryloxy-Z-2-buten-1-ol 
• 128990-34-1 (E)-4-(benzhydryloxy)but-2-enal 

Downstream Products

• 86348-29-0 (4S,5S)-4-Benzhydryloxymethyl-2,2-dimethyl-5-phenylsulfanylmethyl-[1,3]dioxolane 
• 128990-35-2 (2S,3S)-1-Benzhydryloxy-4-thiophenyl-2,3-butanediol 
• 128990-36-3 (4S,5S)-4-Benzenesulfinylmethyl-5-benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolane 
• 1048386-96-4 Acetic acid ((4S,5S)-5-benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-phenylsulfanyl-methyl ester 
• 86348-30-3 (4S,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 86363-76-0 (4R,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 86348-31-4 (E)-3-((4R,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-propenal 
• 86348-32-5 (E)-3-((4S,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-propenal 
• 86348-33-6 [(2R,3R)-3-((4S,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-oxiranyl]-methanol 
• 86348-33-6 [(2S,3S)-3-((4S,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-oxiranyl]-methanol 
• 86348-33-6 [(2R,3R)-3-((4R,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-oxiranyl]-methanol 
• 86348-33-6 [(2S,3S)-3-((4R,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-oxiranyl]-methanol 
• 86348-35-8 (E)-3-((4R,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-prop-2-en-1-ol 
• 86348-35-8 (E)-3-((4S,5S)-5-Benzhydryloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-prop-2-en-1-ol 

Relevant articles and documents

Total synthesis of the L-hexoses

Enantiomerically pure polyhydroxylated natural products are synthesized by using a reiterative two-carbon extension cycle consisting of four key transformations. The generality and efficiency of this methodology are demonstrated in the total synthesis of all eight L-hexoses.