73713-17-4

Basic information

• Product Name: (4S,5S)-2-n-Pentyl-4-(methoxymethyl)-5-phenyl-2-oxazoline
• CAS NO: 73713-17-4
• Molecular Weight: 261.364
• Mol File: 73713-17-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S,5S)-2-n-Pentyl-4-(methoxymethyl)-5-phenyl-2-oxazoline(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S)-2-n-Pentyl-4-(methoxymethyl)-5-phenyl-2-oxazoline(73713-17-4)
• EPA Substance Registry System: (4S,5S)-2-n-Pentyl-4-(methoxymethyl)-5-phenyl-2-oxazoline(73713-17-4)

Safety Data

• Hazardous Substances Data: 73713-17-4(Hazardous Substances Data)

Upstream product

• 28143-91-1 (1S,2S)-2-amino-1-phenyl-1,3-diol 
• 53732-41-5 (4S,5S)-4-Hydroxymethyl-2-methyl-5-phenyl-4,5-dihydro-1,3-oxazole 
• 52075-14-6 (4S,5S)-(-)-4,5-dihydro-4-methoxymethyl-2-methyl-5-phenyloxazole 
• 542-69-8 1-iodo-butane 

Downstream Products

• 73746-63-1 (4S,5S)-4-Methoxymethyl-5-phenyl-2-[1-(2-trimethylsilanyloxy-ethyl)-pentyl]-4,5-dihydro-oxazole 
• 73713-18-5 trans-(4S,5S)-2-(n-pentanoyl)-4-(methoxymethyl)-5-phenyl-2-oxazoline 
• 73746-73-3 (4S,5S)-2-(1-Benzyl-4-trimethylsilanyloxy-butyl)-4-methoxymethyl-5-phenyl-4,5-dihydro-oxazole 
• 73746-77-7 4-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-5-phenyl-pentan-1-ol 
• 73746-72-2 (4S,5S)-4-Methoxymethyl-5-phenyl-2-[1-(3-trimethylsilanyloxy-propyl)-but-3-enyl]-4,5-dihydro-oxazole 
• 73746-71-1 (4S,5S)-4-Methoxymethyl-5-phenyl-2-(1-propyl-4-trimethylsilanyloxy-butyl)-4,5-dihydro-oxazole 
• 73746-70-0 (4S,5S)-2-(1-Ethyl-4-trimethylsilanyloxy-butyl)-4-methoxymethyl-5-phenyl-4,5-dihydro-oxazole 
• 73758-09-5 (4S,5S)-4-Methoxymethyl-2-(1-methyl-4-trimethylsilanyloxy-butyl)-5-phenyl-4,5-dihydro-oxazole 
• 73746-76-6 4-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-hept-6-en-1-ol 
• 73746-69-7 (4S,5S)-2-<4-<(Trimethylsilyl)oxy>butyl>-4-(methoxymethyl)-5-phenyl-2-oxazoline 
• 73713-25-4 (R)-2-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-hexan-2-ol 
• 73746-75-5 4-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-heptan-1-ol 
• 73758-10-8 4-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-hexan-1-ol 
• 73746-74-4 4-((4S,5S)-4-Methoxymethyl-5-phenyl-4,5-dihydro-oxazol-2-yl)-pentan-1-ol 

Relevant articles and documents

Asymmetric Synthesis of 2-Substituted Butyrolactones and Valerolactones

The use of chiral oxazolines 1, 2, 5, and 8 under asymmetrically induced alkylation conditions gave α-substituted oxazolines 3, 6, 9, and 13 which were hydrolyzed to α-substituted butyro- and valerolactones 4 and 11.Either enantiomer of the lactones could be prepared in predictable absolute configuration by reversing the order of alkyl group introduction.The lactones were prepared in 60-86 percent enantiomeric excess which was determined by either chemical correlation or high-pressure liquid chromatography of the diastereomers 10.