24211-53-8

Basic information

• Product Name: 2(3H)-Furanone, 5-(azidomethyl)dihydro-, (S)-
• CAS NO: 24211-53-8
• Molecular Formula: C5H7N3O2
• Molecular Weight: 141.129
• Mol File: 24211-53-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2(3H)-Furanone, 5-(azidomethyl)dihydro-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-Furanone, 5-(azidomethyl)dihydro-, (S)-(24211-53-8)
• EPA Substance Registry System: 2(3H)-Furanone, 5-(azidomethyl)dihydro-, (S)-(24211-53-8)

Safety Data

• Hazardous Substances Data: 24211-53-8(Hazardous Substances Data)

Upstream product

• 32780-06-6 (5S)-5-(hydroxymethyl)-2-oxo-tetrahydrofuran 

Downstream Products

• 102774-92-5 (R)-(+)-5-Hydroxy-2-oxopiperidine 
• 24211-54-9 (S)-5-hydroxypiperidin-2-one 
• 264921-75-7 N-[1-(2'-azido-1'(S)-hydroxy)butylcarboxy]-L-phenylalanyl-L-leucine 
• 24211-55-0 (S)-3-hydroxypiperidine 
• 264921-88-2 N-[1-(2'-[N-tert-butoxycarbonyl-L-tyrosyl]amino-1'(S)-hydroxy)butylcarboxy]-L-phenylalanyl-L-leucyl methyl ester 
• 264921-87-1 N-[1-(2'-amino-1'(S)-hydroxy)butylcarboxy]-L-phenylalanyl-L-leucyl methyl ester 
• 264921-86-0 N-[1-(2'-azido-1'(S)-hydroxy)butylcarboxy]-L-phenylalanyl-L-leucyl methyl ester 

Relevant articles and documents

Concise Enantioselective Synthesis of Naturally Active (S)-3-Hydroxypiperidine

A short and efficient enantioselective synthesis of natural product (S)-3-hydroxypiperidine has been achieved starting from commercially available raw materials employing two catalytic routes: (i) cocatalyzed hydrolytic kinetic resolution (HKR) of racemic methyl-3-(oxiran-2-yl)propanoate; (ii) proline-catalyzed α-aminooxylation followed by Horner-Wardsworth-Emmons olefination in high enantiomeric purity (97% ee) and high overall yield (38%). (Chemical Equation Presented).

Syntheses of (S)-(-)-3-Piperidinol from L-Glutamic Acid and (S)-Malic Acid

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