1323116-61-5

Basic information

• Product Name: tert-butyl 4-(3-hydroxy-3-phenylpropyl)piperazine-1-carboxylate
• CAS NO: 1323116-61-5
• Molecular Weight: 320.432
• Mol File: 1323116-61-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl 4-(3-hydroxy-3-phenylpropyl)piperazine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 4-(3-hydroxy-3-phenylpropyl)piperazine-1-carboxylate(1323116-61-5)
• EPA Substance Registry System: tert-butyl 4-(3-hydroxy-3-phenylpropyl)piperazine-1-carboxylate(1323116-61-5)

Safety Data

• Hazardous Substances Data: 1323116-61-5(Hazardous Substances Data)

Upstream product

• 1323116-50-2 tert-butyl (E)-4-(3-oxo-3-phenylprop-1-en-1-yl)piperazine-1-carboxylate 
• 93-54-9 1-Phenyl-1-propanol 
• 57260-71-6 1-t-Butoxycarbonylpiperazine 
• 936-59-4 3-chloropropiophenone 
• 18776-12-0 3-chloro-1-phenyl-propan-1-ol 
• 62872-58-6 3-iodo-1-phenyl-propan-1-ol 

Downstream Products

• 1373610-98-0 1-(3-phenyl-3-(4-(trifluoromethyl)phenoxy)propyl)piperazine 

Relevant articles and documents

Transformation of α-substituted propanols into γ-amino alcohols through nickel-catalyzed amination on the terminal γ-carbon of propanols

A nickel-phosphine complex was found to be effective as the catalyst for the transformation of alcohols into β-enaminones, which was successively converted into γ-amino alcohols by a conventional reductant. The sequential transformation is equivalent to the carbon-nitrogen bond formation at the γ-position of saturated alcohols. Georg Thieme Verlag Stuttgart · New York.