890655-50-2

Basic information

• Product Name: (R)-benzyl 4-((R)-1-hydroxy-3-oxobutyl)-2,2-dimethyloxazolidine-3-carboxylate
• Synonyms: (R)-benzyl 4-((R)-1-hydroxy-3-oxobutyl)-2,2-dimethyloxazolidine-3-carboxylate
• CAS NO: 890655-50-2
• Molecular Weight: 321.373
• Mol File: 890655-50-2.mol

Chemical Properties

• CAS DataBase Reference: (R)-benzyl 4-((R)-1-hydroxy-3-oxobutyl)-2,2-dimethyloxazolidine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-benzyl 4-((R)-1-hydroxy-3-oxobutyl)-2,2-dimethyloxazolidine-3-carboxylate(890655-50-2)
• EPA Substance Registry System: (R)-benzyl 4-((R)-1-hydroxy-3-oxobutyl)-2,2-dimethyloxazolidine-3-carboxylate(890655-50-2)

Safety Data

• Hazardous Substances Data: 890655-50-2(Hazardous Substances Data)

Upstream product

• 1015081-09-0 C₂₃H₃₇NO₅Si 
• 117833-92-8 (4S)-3-benzyloxycarbonyl-2,2-dimethyloxazolidine-4-carbaldehyde 
• 67-64-1 acetone 

Downstream Products

• 890655-52-4 (R)-benzyl 4-((1R,3S)-1,3-dihydroxybutyl)-2,2-dimethyloxazolidine-3-carboxylate 

Relevant articles and documents

Facile and highly selective deprotection of tert-butyldimethyl silyl ethers using sulfated SnO2 as a solid catalyst

Highly selective deprotection of tert-butyldimethylsilyl ethers at room temperature has been described using sulfated SnO2 as an efficient solid catalyst. Copyright Taylor & Francis Group, LLC.

Stereoselective synthesis of 2-amino-1,3,5-hexane triols using l-proline catalyzed aldol reaction

An efficient synthesis of the 2-amino-1,3,5-hexane triol pattern has been achieved by a diastereoselective aldol reaction of an amino aldehyde with acetone catalyzed by l-proline.