185342-16-9

Basic information

• Product Name: 2-Oxazolidinone, 3-[[3-methoxy-5-(phenylmethoxy)phenyl]acetyl]-4-(phenylmethyl)-, (4S)-
• CAS NO: 185342-16-9
• Molecular Formula: C26H25NO5
• Molecular Weight: 431.488
• Mol File: 185342-16-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Oxazolidinone, 3-[[3-methoxy-5-(phenylmethoxy)phenyl]acetyl]-4-(phenylmethyl)-, (4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Oxazolidinone, 3-[[3-methoxy-5-(phenylmethoxy)phenyl]acetyl]-4-(phenylmethyl)-, (4S)-(185342-16-9)
• EPA Substance Registry System: 2-Oxazolidinone, 3-[[3-methoxy-5-(phenylmethoxy)phenyl]acetyl]-4-(phenylmethyl)-, (4S)-(185342-16-9)

Safety Data

• Hazardous Substances Data: 185342-16-9(Hazardous Substances Data)

Upstream product

• 272457-84-8 (3-benzyloxy-5-methoxy-phenyl)-acetic acid 
• 628330-12-1 methyl (3-benzyloxy-5-methoxyphenyl)acetate 
• 100-39-0 benzyl bromide 
• 4724-10-1 methyl 2-(3,5-dihydroxyphenyl)acetate 
• 101711-90-4 (S)-4-benzyl-2-oxazolidinone lithium salt 

Downstream Products

• 50637-26-8 methyl 3-(benzyloxy)-5-methoxybenzoate 
• 50637-27-9 3-(benzyloxy)-5-methoxybenzoic acid 
• 272457-87-1 (R)-[3-(3-{(S)-[(R)-2-Benzyloxycarbonylamino-3-(4-methoxy-phenyl)-propionylamino]-methylcarbamoyl-methyl}-5-methoxy-phenoxy)-4-methoxy-phenyl]-tert-butoxycarbonylamino-acetic acid 
• 272457-86-0 [(R)-1-{[(S)-(3-Hydroxy-5-methoxy-phenyl)-methylcarbamoyl-methyl]-carbamoyl}-2-(4-methoxy-phenyl)-ethyl]-carbamic acid benzyl ester 
• 272457-85-9 2-amino-2-(3-hydroxy-5-methoxy-phenyl)-N-methyl-acetamide 
• 185342-10-3 (S)-Azido-(3-benzyloxy-5-methoxy-phenyl)-acetic acid 
• 185342-01-2 (S)-3-[(S)-2-Azido-2-(3-benzyloxy-5-methoxy-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one 

Relevant articles and documents

Ruthenium-promoted diaryl ether synthesis in the construction of the F- O-G ring system of a teicoplanin model

An end-game approach is described for the synthesis of glycopeptide antibiotics related to teicoplanin, using ruthenium-promoted diaryl ether formation, followed by cycloamidation. (C) 2000 Elsevier Science Ltd.