121441-79-0

Basic information

• Product Name: <4R,5S>-3-<1-oxo-2-(methoxy)ethyl>-4-methyl-5-phenyl-2-oxazolidinone
• Synonyms: <4R,5S>-3-<1-oxo-2-(methoxy)ethyl>-4-methyl-5-phenyl-2-oxazolidinone
• CAS NO: 121441-79-0
• Molecular Weight: 249.266
• Mol File: 121441-79-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: <4R,5S>-3-<1-oxo-2-(methoxy)ethyl>-4-methyl-5-phenyl-2-oxazolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: <4R,5S>-3-<1-oxo-2-(methoxy)ethyl>-4-methyl-5-phenyl-2-oxazolidinone(121441-79-0)
• EPA Substance Registry System: <4R,5S>-3-<1-oxo-2-(methoxy)ethyl>-4-methyl-5-phenyl-2-oxazolidinone(121441-79-0)

Safety Data

• Hazardous Substances Data: 121441-79-0(Hazardous Substances Data)

Upstream product

• 37577-28-9 (1S,2R)-(+)-norphedrine 
• 159164-17-7 lithium (4R,5S)-(+)-4-methyl-5-phenyl-2-oxazolidinone 
• 625-45-6 2-methoxyacetic acid 
• 77943-39-6 4-methyl-5-phenyloxazolidin-2-one 
• 38870-89-2 Methoxyacetyl chloride 

Downstream Products

• 1264175-76-9 (4R,5S)-3-((2R,3S,E)-3-hydroxy-2,8-dimethoxy-4-methyloct-4-enoyl)-4-methyl-5-phenyloxazolidin-2-one 
• 121441-86-9 <4R-<3(2S^*,3S^*),4α,5α>>-methyl 2-<<2-methoxy-3-(4-methyl-2-oxo-5-phenyl-3-oxazolidinyl)-3-oxo-1-<2-(8-phenyloctyl)phenyl>propyl>thio>propanoate 
• 175356-50-0 (4R,5S)-3-{(E)-(2R,3S,6S)-6-[(2R,3S,5S,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-3-methoxy-5-methyl-tetrahydro-pyran-2-yl]-3-hydroxy-2-methoxy-4-methyl-hept-4-enoyl}-4-methyl-5-phenyl-oxazolidin-2-one 
• 161985-42-8 (4R,5S)-3-((S)-3-Benzyloxy-2-methoxy-propionyl)-4-methyl-5-phenyl-oxazolidin-2-one 
• 121441-80-3 <4R-<3(2R^*,3S^*),4α,5α>>-3-<3-hydroxy-2-methoxy-1-oxo-3-<2-(8-phenyloctyl)phenyl>propyl>-4-methyl-5-phenyl-2-oxozolidinone 

Relevant articles and documents

Novel approach to the ansamycin antibiotics macbecin I and herbimycin A. A formal total synthesis of (+)-macbecin I

The asymmetric syntheses of 25 and 29, which constitutes the C(3)-C(15) segment of the stereochemically complex ansa chain of (+)-macbecin I (1) and herbimycin A (2), respectively, have been achieved. The approach features the furan-hydropyranone transfor