120020-02-2

Basic information

• Product Name: (+/-)-2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-3-phenylpropanoic acid benzyl ester
• Synonyms: (+/-)-2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-3-phenylpropanoic acid benzyl ester
• CAS NO: 120020-02-2
• Molecular Weight: 470.566
• Mol File: 120020-02-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (+/-)-2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-3-phenylpropanoic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-3-phenylpropanoic acid benzyl ester(120020-02-2)
• EPA Substance Registry System: (+/-)-2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-3-phenylpropanoic acid benzyl ester(120020-02-2)

Safety Data

• Hazardous Substances Data: 120020-02-2(Hazardous Substances Data)

Upstream product

• 870-50-8 di-tert-butyl-diazodicarboxylate 
• 501-52-0 3-Phenylpropionic acid 
• 100-51-6 benzyl alcohol 
• 22767-96-0 Benzyl 3-phenylpropionate 
• 15082-42-5 lithium benzyloxide 
• 104266-94-6 (3(2S),4S)-3-(2-(N,N'-bis-(t-butoxycarbonyl)hydrazino)-3-phenyl-1-oxopropyl)-4-(phenylmethyl)-2-oxazolidinone 

Downstream Products

• 63-91-2 L-phenylalanine 
• 1202-31-9 (S)-2-hydrazinyl-3-phenylpropanoic acid 
• 1202-30-8 D-α-Hydrazino-β-phenyl-propionsaeure 

Relevant articles and documents

Electrophilic amination of ketone enolates mediated by the DiTOX asymmetric building block: Enantioselective formal synthesis of α-aminoacids

Diastereoselective electrophilic amination of enolates derived from 2-acyl-1,3-dithiane 1-oxides is used as the key step for an enantioselective synthesis of two α-hydrazido carboxylic acids, well-known precursors of α-amino acids. (C) 2000 Elsevier Science Ltd.

Amination of Chiral Enolates by Dialkyl Azodiformates. Synthesis of α-Hydrazino Acids and α-Amino Acids

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