155905-73-0

Basic information

• Product Name: [(R)-1-(1-Benzenesulfonyl-cyclobutyl)-2-(tetrahydro-pyran-2-yloxy)-ethyl]-carbamic acid tert-butyl ester
• CAS NO: 155905-73-0
• Molecular Weight: 439.573
• Mol File: 155905-73-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(R)-1-(1-Benzenesulfonyl-cyclobutyl)-2-(tetrahydro-pyran-2-yloxy)-ethyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(R)-1-(1-Benzenesulfonyl-cyclobutyl)-2-(tetrahydro-pyran-2-yloxy)-ethyl]-carbamic acid tert-butyl ester(155905-73-0)
• EPA Substance Registry System: [(R)-1-(1-Benzenesulfonyl-cyclobutyl)-2-(tetrahydro-pyran-2-yloxy)-ethyl]-carbamic acid tert-butyl ester(155905-73-0)

Safety Data

• Hazardous Substances Data: 155905-73-0(Hazardous Substances Data)

Upstream product

• 116611-45-1 (2R)-2-t-butoxycarbonylamino-3-phenylsulfonyl-1-(2-tetrahydropyranyloxy)propane 
• 109-70-6 1.3-chlorobromopropane 

Downstream Products

• 155905-77-4 (S)-tert-Butoxycarbonylamino-cyclobutyl-acetic acid 

Relevant articles and documents

A Versatile Method for the Synthesis of (S)- or (R)-Cycloalkylglycines, (S)- or (R)-N-Heterocyclic and α,β-Unsaturated N-Heterocyclic α-Amino Acids

Two different types of cyclic α-amino acids, cycloalkylglycines and N-heterocyclic α-amino acids, were prepared in optically pure form from the same chiral synthon 1-(R) (or 1-(S)) simply by altering the quantity or type of base required for anion formation.Elaboration of the heterocyclic intermediate 3 provided α,β-unsaturated N-heterocyclic α-amino acids.