1637370-47-8

Basic information

• Product Name: (R)-5-benzyl-5-(iodomethyl)dihydrofuran-2(3H)-one
• Synonyms: (R)-5-benzyl-5-(iodomethyl)dihydrofuran-2(3H)-one
• CAS NO: 1637370-47-8
• Molecular Weight: 316.139
• Mol File: 1637370-47-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-5-benzyl-5-(iodomethyl)dihydrofuran-2(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-5-benzyl-5-(iodomethyl)dihydrofuran-2(3H)-one(1637370-47-8)
• EPA Substance Registry System: (R)-5-benzyl-5-(iodomethyl)dihydrofuran-2(3H)-one(1637370-47-8)

Safety Data

• Hazardous Substances Data: 1637370-47-8(Hazardous Substances Data)

Upstream product

• 1282061-34-0 4-benzylpent-4-enoic acid 
• 1312844-96-4 ethyl 4-benzylpent-4-enoate 
• 20416-11-9 Ethyl 4-oxo-5-phenyl-pentanoate 
• 6921-34-2 benzylmagnesium chloride 

Downstream Products

• 1637370-62-7 C₁₄H₁₆O₄ 
• 1637370-37-6 (S)-methyl 2-benzyltetrahydrofuran-2-carboxylate 
• 1024613-09-9 (S)-5-benzyl-5-(hydroxymethyl)dihydrofuran-2(3H)-one 

Relevant articles and documents

Cooperative activation with chiral nucleophilic catalysts and n-haloimides: Enantioselective iodolactonization of 4-arylmethyl-4-pentenoic acids

Chiral triaryl phosphates promote the enantioselective iodolactonization of 4-substituted 4-pentenoic acids to give the corresponding iodolactones in high yields with high enantioselectivity. N-Chlorophthalimide (NCP) is employed as a Lewis acidic activat