1369415-68-8

Basic information

• Product Name: methyl 6-((1S,2R,6S)-2-((S)-4-benzyl-2-oxooxazolidine-3-carbonyl)-1-hydroxy-6-methyloctyl)phenazine-1-carboxylate
• Synonyms: methyl 6-((1S,2R,6S)-2-((S)-4-benzyl-2-oxooxazolidine-3-carbonyl)-1-hydroxy-6-methyloctyl)phenazine-1-carboxylate
• CAS NO: 1369415-68-8
• Molecular Weight: 583.684
• Mol File: 1369415-68-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 6-((1S,2R,6S)-2-((S)-4-benzyl-2-oxooxazolidine-3-carbonyl)-1-hydroxy-6-methyloctyl)phenazine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 6-((1S,2R,6S)-2-((S)-4-benzyl-2-oxooxazolidine-3-carbonyl)-1-hydroxy-6-methyloctyl)phenazine-1-carboxylate(1369415-68-8)
• EPA Substance Registry System: methyl 6-((1S,2R,6S)-2-((S)-4-benzyl-2-oxooxazolidine-3-carbonyl)-1-hydroxy-6-methyloctyl)phenazine-1-carboxylate(1369415-68-8)

Safety Data

• Hazardous Substances Data: 1369415-68-8(Hazardous Substances Data)

Upstream product

• 1336882-47-3 methyl 6-formylphenazine-1-carboxylate 
• 1369415-67-7 (S)-4-benzyl-3-((S)-6-methyloctanoyl)oxazolidin-2-one 
• 504-99-4 (6S)-6-methyloctanoic acid 
• 110453-78-6 (S)-(+)-6-methyl-1-octanol 

Relevant articles and documents

Asymmetric synthesis and absolute configuration of streptophenazine G

The asymmetric synthesis of the antibacterial natural product, streptophenazine G, has been achieved by employing asymmetric alkylation and asymmetric aldol reactions using chiral oxazolidinones as the key steps. The originally proposed structure for streptophenazine G has been revised, and its absolute configuration has been determined to be 1′S,2′R,6′S. The asymmetric total synthesis of 6′-epi-streptophenazine G is also described.