125763-09-9

Basic information

• Product Name: 3-benzyl-4-(bromomethyl)oxetan-2-one
• Synonyms: 3-benzyl-4-(bromomethyl)oxetan-2-one
• CAS NO: 125763-09-9
• Molecular Weight: 255.111
• Mol File: 125763-09-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-benzyl-4-(bromomethyl)oxetan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-benzyl-4-(bromomethyl)oxetan-2-one(125763-09-9)
• EPA Substance Registry System: 3-benzyl-4-(bromomethyl)oxetan-2-one(125763-09-9)

Safety Data

• Hazardous Substances Data: 125763-09-9(Hazardous Substances Data)

Upstream product

• 90252-79-2 3-benzylbut-3-enoic acid 

Downstream Products

• 125763-14-6 1-phenyl-cis-3-benzyl-pr4-hydroxy-2-pyrrolidinone 
• 935-00-2 trans-4-phenyl-2-butene 
• 768-56-9 4-Phenylbut-1-ene 
• 15324-90-0 (2Z)-but-2-en-1-ylbenzene 
• 125763-12-4 3-phenyl-5(S')-<1'(S')-(methoxycarbonyl)2'-phenylethyl>-1,3-oxazolidin-2-one 
• 78986-57-9 α-Benzyl-β-hydroxy-γ-butyrolactone 

Relevant articles and documents

Synthesis of Heterocyclic Compounds by the Organotin Alkoxide Promoted Cleavage of γ-Bromo β-Lactones

A variety of 2-oxazolidinones are prepared in good to excellent yields by the organotin alkoxide promoted ring cleavage of γ-bromo β-lactones.This reaction proceeds via the key organotin haloalkoxide intermediate, which reacts with an isocyanate followed by cyclization.Stereoisomerically pure products are obtained by combination with the stereoselective bromolactonization reaction.Moreover, other heterocumulenes such as RN=C=NR, RN=C=S, CO2, and γ-bromo β-lactam are used as substrates.