85390-46-1

Basic information

• Product Name: 1-Benzyl-4-(hydroxymethyl)azetidin-2-one
• Synonyms: 1-Benzyl-4-(hydroxymethyl)azetidin-2-one
• CAS NO: 85390-46-1
• Molecular Weight: 191.23
• Mol File: 85390-46-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Benzyl-4-(hydroxymethyl)azetidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Benzyl-4-(hydroxymethyl)azetidin-2-one(85390-46-1)
• EPA Substance Registry System: 1-Benzyl-4-(hydroxymethyl)azetidin-2-one(85390-46-1)

Safety Data

• Hazardous Substances Data: 85390-46-1(Hazardous Substances Data)

Upstream product

• 86694-80-6 ethyl 4-oxo-1-(phenylmethyl)-2-azetidinecarboxylate 
• 337522-48-2 1-benzyl-4-(tert-butyldimethylsilyloxymethyl)azetidin-2-one 
• 78159-38-3 1-Benzyl-4-oxo-azetidine-2-carboxylic acid methyl ester 
• 16940-66-2 sodium tetrahydroborate 
• 86694-78-2 diethyl N-benzyl-N-(chloroacetyl)aminomalonate 
• 86694-79-3 diethyl 1-benzyl-4-oxoazetidine-2,2-dicarboxylate 
• 56598-99-3 diethyl 2-(benzylamino)malonate hydrochloride 
• 39919-84-1 1-benzyl-4-vinylazetidin-2-one 

Downstream Products

• 1613228-93-5 1-benzyl-4-cyanomethyl-β-lactam 
• 1613229-15-4 C₁₂H₁₄N₂O₂ 
• 1613229-02-9 C₁₂H₁₄N₂O₂ 
• 80974-44-3 (S)-N-benzyl-4-carboxymethyl-2-azetidinone 
• 76144-17-7 (4R) N-Benzyl-4-methoxycarbonylmethyl-azetidin-2-one 
• 85390-48-3 1-Benzyl-4-(iodomethyl)azetidin-2-one 
• 85390-58-5 but-3-enoic acid benzylamide 
• 89232-30-4 (2E)-N-benzylbut-2-enamide 
• 4391-83-7 1-benzyl-4-methylazetidinone 
• 85390-47-2 1-Benzyl-4-(p-tosyloxymethyl)azetidin-2-one 
• 86694-81-7 1-benzyl-4-(mesyloxymethyl)-2-azetidinone 

Relevant articles and documents

Efficient synthesis of highly enantiopure β-lactam derivatives from biocatalytic transformations of amides and nitriles

Catalyzed by Rhodococcus erythropolis AJ270, a nitrile hydratase and amidase containing microbial strain, under mild conditions, kinetic resolution of racemic amides provides an efficient and scalable route to highly enantioenriched R-4-carboxymethyl-β-la

Simple and condensed β-lactams. II. The synthesis of new diethyl 4-oxoazetidine-2,2-dicarboxylates and some manipulations of their functional groups and N-substituents

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Reaction of 4-(Iodomethyl)azetidin-2-ones with Tetracarbonylferrate(-II)

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