17623-72-2

Basic information

• Product Name: 2-methyl-4-iso-propyl-4H-oxazolin-5-one
• CAS NO: 17623-72-2
• Molecular Weight: 141.17
• Mol File: 17623-72-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-methyl-4-iso-propyl-4H-oxazolin-5-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-4-iso-propyl-4H-oxazolin-5-one(17623-72-2)
• EPA Substance Registry System: 2-methyl-4-iso-propyl-4H-oxazolin-5-one(17623-72-2)

Safety Data

• Hazardous Substances Data: 17623-72-2(Hazardous Substances Data)

Upstream product

• 96-81-1 N-acetyl-D,L-valine 
• 541-41-3 chloroformic acid ethyl ester 
• 4090-17-9 racemic N-chloroacetylvaline 
• 145985-01-9 N-<α-(acetylamino)isovaleryl>imidazole 
• 96-81-1 N-acetyl-L-valine 
• 108-24-7 acetic anhydride 
• 516-06-3 D,L-valine 
• 4894-12-6 4-isopropylidene-2-methyloxazol-5(4H)-one 

Downstream Products

• 85642-18-8 (R)-2-Acetylamino-3-methyl-N-((S)-1-phenyl-ethyl)-butyramide 
• 81019-01-4 (S)-2-Acetylamino-3-methyl-N-((S)-1-phenyl-ethyl)-butyramide 
• 96574-46-8 N²-<(R)-N²-acetylvalyl>-L-phenylalanine dimethylamide 
• 96574-45-7 N²-<(S)-N²-acetylvalyl>-L-phenylalanine dimethylamide 
• 1394018-10-0 N-(3-methyl-1-(4-nitrophenyl)-1-oxobutan-2-yl)acetamide 
• 96-81-1 N-acetyl-L-valine 
• 17916-88-0 N-acetyl-D-valine 

Relevant articles and documents

BENZAMIDE TRPA1 ANTAGONISTS

Compounds of formula I, pharmaceutically acceptable salts thereof, diastereomers, enantiomers, or mixtures thereof: wherein R, X, Y, Z, n and A are as defined in the specification, as well as pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.

Diastereochemical diversity of imidazoline scaffolds via substrate controlled TMSCI mediated cycloaddition of azlactones

(Chemical Equation Presented) We report herein a trimethylsilyl chloride mediated substrate controlled 1,3-dipolar cycloaddition for the diastereoselective synthesis of either syn- or anti-imidazolines. This method provides scaffolds with four points of diversity and control over two stereocenters.

Intramolecular Participation by a Neighboring Amide Group in the Hydrolysis of N-Acylimidazoles

Rate constants have been determined for the disappearance of the N-acylimidazole derivatives of N-acetylphenylalanine and N-acetylvaline in H2O at 30 deg C.The pH-rate constant profiles are characterized by large pH-independent regions.These reactions are