501031-61-4

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 
• 55-21-0 benzamide 
• 30414-53-0 methyl propanoyl acetate 

Downstream Products

• 1262547-45-4 (R)-methyl 2-hydroxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1262547-46-5 (S)-methyl 2-hydroxy-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1334871-98-5 (S)-methyl 3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)-2-phenoxypropanoate 
• 1334872-00-2 (S)-methyl 3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)-2-(pyridin-3-yloxy)propanoate 
• 1262547-50-1 (S)-methyl 2-(4-fluorophenoxy)-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1334872-05-7 (S)-methyl 2-(3-fluorophenoxy)-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1334872-07-9 (S)-methyl 3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)-2-(3,4,5-trifluorophenoxy)propanoate 
• 1262547-51-2 (S)-methyl 2-(4-bromophenoxy)-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1334872-10-4 (S)-methyl 2-(2-bromophenoxy)-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1262547-52-3 (S)-methyl 2-(4-chlorophenoxy)-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1334872-13-7 (S)-methyl 2-(2,4-dichlorophenoxy)-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1334872-14-8 (S)-methyl 2-(3-iodophenoxy)-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1262547-53-4 (S)-methyl 2-(4-iodophenoxy)-3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)propanoate 
• 1334872-17-1 (S)-methyl 3-(2-(3-(5-methyl-2-phenyloxazol-4-yl)propyl)benzo[d]oxazol-5-yl)-2-(4-(trifluoromethyl)phenoxy)propanoate 

Relevant academic research and scientific papers

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