132553-76-5

Basic information

• Product Name: [(2S,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester
• CAS NO: 132553-76-5
• Molecular Weight: 518.055
• Mol File: 132553-76-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(2S,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(2S,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester(132553-76-5)
• EPA Substance Registry System: [(2S,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester(132553-76-5)

Safety Data

• Hazardous Substances Data: 132553-76-5(Hazardous Substances Data)

Upstream product

• 132553-76-5 [(2R,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester 
• 127822-76-8 (+/-)-erythro-β-chloro-γ-hydroxy-1-triphenylmethyl-1H-4-imidazolepropanamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 132553-77-6 [2-Chloro-3-oxo-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester 

Downstream Products

• 110883-46-0 (+/-)-threo-2-amino-β-chloro-γ-hydroxy-1H-4-imidazolepropanamine 
• 132553-74-3 {(2S,3S)-2-Chloro-3-[2-(4-chloro-phenylazo)-1H-imidazol-4-yl]-3-hydroxy-propyl}-carbamic acid tert-butyl ester 
• 127822-76-8 (1S,2S)-3-Amino-2-chloro-1-(1-trityl-1H-imidazol-4-yl)-propan-1-ol 
• 134822-16-5 (5S,6S)-5-Chloro-6-(1-trityl-1H-imidazol-4-yl)-[1,3]oxazinan-2-one 
• 132553-76-5 [(2S,3S)-2-Chloro-3-hydroxy-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester 
• 132553-77-6 [2-Chloro-3-oxo-3-(1-trityl-1H-imidazol-4-yl)-propyl]-carbamic acid tert-butyl ester 

Relevant articles and documents

A diastereoselective synthesis of girolline

Girolline (RP 49532, 1), a new antitumour agent, was prepared in the racemic series using an oxidation-reduction sequence starting from (±)-erythro-β-chloro-γ-hydroxy- 1-triphenylmethyl-1H-4-imidazolepropanamine 3. The heterocyclic amino function was intr