779289-59-7

Basic information

• Product Name: 4-Oxazolecarboxylicacid,4,5-dihydro-5-methyl-2-phenyl-,(4S-trans)-(9CI)
• Synonyms: 4-Oxazolecarboxylicacid,4,5-dihydro-5-methyl-2-phenyl-,(4S-trans)-(9CI)
• CAS NO: 779289-59-7
• Molecular Formula: C11H11NO3
• Molecular Weight: 0
• Product Categories: METHYL
• Mol File: 779289-59-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Oxazolecarboxylicacid,4,5-dihydro-5-methyl-2-phenyl-,(4S-trans)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Oxazolecarboxylicacid,4,5-dihydro-5-methyl-2-phenyl-,(4S-trans)-(9CI)(779289-59-7)
• EPA Substance Registry System: 4-Oxazolecarboxylicacid,4,5-dihydro-5-methyl-2-phenyl-,(4S-trans)-(9CI)(779289-59-7)

Safety Data

• Hazardous Substances Data: 779289-59-7(Hazardous Substances Data)

Upstream product

• 115246-64-5 (2S,3S)-erythro-N-benzoyl-threonine 
• 825-60-5 benzimidic acid ethyl ester 
• 7462-66-0 5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid ethyl ester 
• 7462-66-0 5c-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid ethyl ester 
• 72-19-5 rac-allo-threonine 
• 100-47-0 benzonitrile 
• 99843-24-0 (4S)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid 
• 27696-01-1 (2S,3R)-threo-N-benzoyl-threonine 
• 79893-89-3 N-benzoyl-L-threonine methyl ester 
• 82659-84-5 (4S,5S)-5-methyl-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 
• 141-52-6 sodium ethanolate 
• 99843-24-0 (+/-)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid 
• 60538-17-2 (4S,5R)-4-methyl-2-phenyl-4,5-dihydrooxazole-4-carboxylic acid methyl ester 

Downstream Products

• 27696-01-1 (2S,3R)-threo-N-benzoyl-threonine 
• 99843-24-0 (4R)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid 
• 906324-06-9 N-benzoyl-D_s-threonine 
• 79893-89-3 N-benzoyl-L-threonine methyl ester 
• 82659-84-5 (4S,5S)-5-methyl-2-phenyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 

Relevant articles and documents

Structure-activity relationship of new anti-tuberculosis agents derived from oxazoline and oxazole benzyl esters

During the syntheses and studies of natural iron chelators (mycobactins), we serendipitously discovered that a simple, small molecule, oxazoline-containing intermediate 3 displayed surprising anti-tuberculosis activity (MIC of 7.7?μM, average). Herein we