246158-05-4

Basic information

• Product Name: (4S,5R)-5-Allyl-4-(4-tert-butoxy-benzyl)-oxazolidin-2-one
• CAS NO: 246158-05-4
• Molecular Weight: 289.375
• Mol File: 246158-05-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S,5R)-5-Allyl-4-(4-tert-butoxy-benzyl)-oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5R)-5-Allyl-4-(4-tert-butoxy-benzyl)-oxazolidin-2-one(246158-05-4)
• EPA Substance Registry System: (4S,5R)-5-Allyl-4-(4-tert-butoxy-benzyl)-oxazolidin-2-one(246158-05-4)

Safety Data

• Hazardous Substances Data: 246158-05-4(Hazardous Substances Data)

Upstream product

• 246158-03-2 benzyl (1S,2R)-1-(4-tert-butoxybenzyl)-2-hydroxypent-4-enylcarbamate 
• 5068-29-1 2-benzyloxycarbonylamino-3-(4-tert-butoxy-phenyl)-propionic acid methyl ester 
• 109953-91-5 [1-(4-tert-butoxy-benzyl)-2-hydroxy-ethyl]-carbamic acid benzyl ester 

Downstream Products

• 246158-09-8 (2S,3R)-2-Azido-1-(4-tert-butoxy-phenyl)-hex-5-en-3-ol 
• 246158-08-7 (2S,3R)-2-Amino-1-(4-tert-butoxy-phenyl)-hex-5-en-3-ol 

Relevant articles and documents

Synthesis of a novel β-turn mimetic and its incorporation in Leu- enkephalin

A conformationally restricted β-turn mimetic, in which an ethylene bridge replaces the intramolecular hydrogen bond between residues i and i+3 of β-turns, has been prepared and incorporated in Leu-enkephalin. Amino acids and α-bromoacids were used as building blocks in the synthesis of the mimetic.