75866-73-8

Basic information

• Product Name: (S)-2-ethyl-4,5-dihydro-4-(phenylmethyl)oxazole
• Synonyms: (S)-2-ethyl-4,5-dihydro-4-(phenylmethyl)oxazole
• CAS NO: 75866-73-8
• Molecular Weight: 189.257
• Mol File: 75866-73-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-2-ethyl-4,5-dihydro-4-(phenylmethyl)oxazole(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-ethyl-4,5-dihydro-4-(phenylmethyl)oxazole(75866-73-8)
• EPA Substance Registry System: (S)-2-ethyl-4,5-dihydro-4-(phenylmethyl)oxazole(75866-73-8)

Safety Data

• Hazardous Substances Data: 75866-73-8(Hazardous Substances Data)

Upstream product

• 73058-30-7 (2S)-2-benzylazacyclopropane 
• 131685-53-5 (S)-4-benzyl-3-propionyl-2-oxazolidinone 
• 63-91-2 L-phenylalanine 
• 24823-81-2 trimethoxypropane 
• 3182-95-4 L-Phenylalaninol 
• 75866-62-5 (+)-1-(propanoyl)-2(S)-benzylaziridine 

Downstream Products

• 1285526-93-3 propionic acid (E)-2-hydroxyimino-3-phenylpropyl ester 
• 1285526-87-5 propionic acid (Z)-2-hydroxyimino-3-phenylpropyl ester 
• 1285526-80-8 C₂₄H₃₀N₂O₆ 
• 195198-29-9 (S)-4-benzyl-1-phenyl-3-propionylimidazolidin-2-one 
• 195198-36-8 (S)-4-benzyl-1-phenyl-3-(3-phenylpropionyl)imdazolidin-2-one 
• 195198-33-5 (4S)-1-phenyl-4-phenylmethyl-2-imidazolidinone 
• 195198-22-2 (S)-N-[1-phenyl-3-(phenylamino)prop-2-yl]propionamide 

Relevant articles and documents

Azodioxy-carbonyl compounds by oxidation of cyclic imines with m-CPBA

This article reports a simple and efficient synthesis of C-nitroso compounds (azodioxy esters or ketones and oximes) through a double oxidation of cyclic imines (4,5-dihydrooxazoles and 3,4-dihydro-2H-pyrroles) with m-CPBA. C-Nitroso derivatives seem to b

A mild, general preparation of N-acyl aziridines and 2-substituted 4(S)-benzyloxazolines

The conversion of a wide range of carboxylic acids into their acyl imidazolides with subsequent addition of an aziridine rapidly gives a quantitative yield of the corresponding N-acyl aziridines.Iodide (or bromide) ion catalysed rearrangement of N-acyl 2(S)-benzylaziridines 1 to oxazolines 6 proceeds quantitatively.