135387-93-8

Basic information

• Product Name: (S)-3-[(S)-2-Azido-2-(3,5-dimethoxy-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one
• Synonyms: (S)-3-[(S)-2-Azido-2-(3,5-dimethoxy-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one
• CAS NO: 135387-93-8
• Molecular Weight: 396.403
• Mol File: 135387-93-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-3-[(S)-2-Azido-2-(3,5-dimethoxy-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-[(S)-2-Azido-2-(3,5-dimethoxy-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one(135387-93-8)
• EPA Substance Registry System: (S)-3-[(S)-2-Azido-2-(3,5-dimethoxy-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one(135387-93-8)

Safety Data

• Hazardous Substances Data: 135387-93-8(Hazardous Substances Data)

Upstream product

• 4724-10-1 methyl 2-(3,5-dihydroxyphenyl)acetate 
• 4670-10-4 (3,5-dimethoxyphenyl)acetic acid 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 6512-32-9 methyl 2-(3,5-dimethoxyphenyl)acetate 
• 4670-09-1 2-(3,5-dihydroxyphenyl)acetic acid 
• 135387-90-5 (S)-4-Benzyl-3-[2-(3,5-dimethoxy-phenyl)-acetyl]-oxazolidin-2-one 

Downstream Products

• 141362-63-2 [(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3,5-dimethoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester 
• 103889-87-8 (S)-3,5-dimethoxyphenylglycine 
• 103889-85-6 (R)-3,5-dimethoxyphenylglycine 
• 141362-64-3 (S)-tert-Butoxycarbonylamino-(3,5-dimethoxy-phenyl)-acetic acid 

Relevant articles and documents

A General Approach to the Asymmetric Synthesis of Vancomycin-Related Arylglycines by Enolate Azidation

The asymmetric synthesis of vancomycin-related α-azido arylglycines by direct azide transfer methodology is reported.Procedures for the conversion of the azides to N-protected arylglycines are provided.