1247010-90-7

Basic information

• Product Name: (S)-2-methoxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoic acid
• Synonyms: (S)-2-methoxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoic acid
• CAS NO: 1247010-90-7
• Molecular Weight: 420.465
• Mol File: 1247010-90-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-methoxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-methoxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoic acid(1247010-90-7)
• EPA Substance Registry System: (S)-2-methoxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoic acid(1247010-90-7)

Safety Data

• Hazardous Substances Data: 1247010-90-7(Hazardous Substances Data)

Upstream product

• 105983-77-5 methyl 4-bromo-3-oxopentanoate 
• 103788-64-3 methyl 2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)acetate 
• 103788-65-4 (5-methyl-2-phenyloxazol-4-yl)ethanol 
• 55-21-0 benzamide 
• 38196-09-7 3-(4-hydroxy-3-nitrophenyl)propionic acid 
• 501-97-3 4-hydroxyphenylpropionic acid 
• 30414-53-0 methyl propanoyl acetate 
• 1262547-44-3 (S)-3-((S)-2-hydroxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoyl)-4-isopropyl oxazolidin-2-one 
• 1262547-42-1 (S)-4-isopropyl-3-(3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoyl)oxazolidin-2-one 
• 1262547-40-9 3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoic acid 
• 1262547-39-6 methyl 3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1262547-38-5 methyl 3-(2-((diethoxyphosphoryl)methyl)benzo[d]oxazol-5-yl)propanoate 
• 1247011-54-6 (S)-methyl 2-methoxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1262547-37-4 methyl 3-(2-(chloromethyl)benzo[d]oxazol-5-yl)propanoate 

Relevant articles and documents

Design, synthesis and antimicrobial activity of chiral 2-(substituted- hydroxyl)-3-(benzo[d]oxazol-5-yl)propanoic acid derivatives

Chiral 2-(substituted-hydroxyl)-3-(benzo[d]oxazol-5-yl)propanoic acid derivatives were synthesized and their antibacterial activities were evaluated against fungus, Gram-negative and Gram-positive bacteria. In general, these compounds showed in vitro acti