87436-78-0

Basic information

• Product Name: Phosphonium, (4-hydroxybutyl)triphenyl-, bromide
• CAS NO: 87436-78-0
• Molecular Formula: C22H24OP.Br
• Molecular Weight: 415.31
• Mol File: 87436-78-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phosphonium, (4-hydroxybutyl)triphenyl-, bromide(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonium, (4-hydroxybutyl)triphenyl-, bromide(87436-78-0)
• EPA Substance Registry System: Phosphonium, (4-hydroxybutyl)triphenyl-, bromide(87436-78-0)

Safety Data

• Hazardous Substances Data: 87436-78-0(Hazardous Substances Data)

Upstream product

• 89043-32-3 (4-bromobutoxy)-tert-butyldimethylsilane 
• 603-35-0 triphenylphosphine 
• 33036-62-3 4-Bromo-1-butanol 

Downstream Products

• 13159-16-5 (Z)-5-phenylpent-4-en-1-ol 
• 13159-16-5 (E)-5-phenyl-4-penten-1-ol 
• 13159-16-5 5-phenyl-4-penten-1-ol 
• 1426692-66-1 3-chloro-2-o-tolyltetrahydro-2H-pyran 
• 105337-73-3 (E)-5-o-tolylpent-4-en-1-ol 
• 139929-07-0 Lithium; 4-(triphenyl-λ⁵-phosphanylidene)-pentan-1-olate 
• 16695-34-4 (E)-4-none-1-ol 

Relevant articles and documents

Copper-Catalyzed Diastereoselective Synthesis of Trifluoromethylated Tetrahydrofurans

The copper-catalyzed intramolecular diastereoselective trifluoromethylcycloetherification of homoallylic alcohols with Togni's reagent as trifluoromethylating reagent was realized under mild conditions. Various trifluoromethylated tetrahydrofurans were synthesized in moderate to good yields. Moreover, a wide range of common functional groups was tolerated.

Constituents of holothuroidea, 16. Determination of absolute configuration of the branched methyl group in ante-iso type side chain moiety on long chain base of glucocerebroside from the sea cucumber Holothuria leucospilota

The absolute configuration of the branched methyl group in ante-iso type side chain moiety on the long chain base of glucocerebroside, HLC-2-A, which was isolated from the sea cucumber Holothuria leucospilota was determined. Oxidation of the glucocerebros