99843-24-0

Basic information

• Product Name: (4S)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid
• Synonyms: (4S)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid
• CAS NO: 99843-24-0
• Molecular Weight: 205.213
• Mol File: 99843-24-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4S)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid(99843-24-0)
• EPA Substance Registry System: (4S)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid(99843-24-0)

Safety Data

• Hazardous Substances Data: 99843-24-0(Hazardous Substances Data)

Upstream product

• 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 
• 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 
• 99843-24-0 (4S)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid 
• 27696-01-1 (2S,3R)-threo-N-benzoyl-threonine 

Downstream Products

• 72-19-5 L-threonine 
• 27696-01-1 (2S,3R)-threo-N-benzoyl-threonine 
• 99843-24-0 (4S)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid 
• 99843-24-0 (4R)-5t-methyl-2-phenyl-4,5-dihydro-oxazole-4r-carboxylic acid 
• 956591-66-5 C₁₁H₁₂N₂O₂ 
• 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 
• 956591-69-8 C₁₁H₁₄N₂O 
• 906324-06-9 N-benzoyl-D_s-threonine 

Relevant articles and documents

Oxazoline-thiourea as a bifunctional organocatalyst: Enantioselective aza-Henry reactions

Bifunctional oxazoline-thiourea-based organocatalysts were synthesized and applied to the aza-Henry reactions between N-Boc aryl imines and nitromethane in high ee and chemical yields at room temperature. Georg Thieme Verlag Stuttgart.