438470-79-2

Basic information

• Product Name: (R)-dibenzyl 1-(1-hydroxy-3-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate
• Synonyms: (R)-dibenzyl 1-(1-hydroxy-3-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate
• CAS NO: 438470-79-2
• Molecular Weight: 434.492
• Mol File: 438470-79-2.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: (R)-dibenzyl 1-(1-hydroxy-3-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-dibenzyl 1-(1-hydroxy-3-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate(438470-79-2)
• EPA Substance Registry System: (R)-dibenzyl 1-(1-hydroxy-3-phenylpropan-2-yl)hydrazine-1,2-dicarboxylate(438470-79-2)

Safety Data

• Hazardous Substances Data: 438470-79-2(Hazardous Substances Data)

Upstream product

• 1064655-01-1 C₂₅H₂₄N₂O₅ 
• 104-53-0 3-phenyl-propionaldehyde 
• 2449-05-0 dibenzyl azodicarboxylate 
• 2449-05-0 dibenzyl azodicarboxylate 

Downstream Products

• 5267-64-1 (R)-2-amino-3-phenylpropanol 
• 106454-69-7 N-tert-butoxycarbonyl-D-Phenylalaninol 
• 40217-17-2 (R)-4-(phenylmethyl)-2-oxazolidinone 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 

Relevant articles and documents

Organocatalyst Efficiency in the α-Aminoxylation and α-Hydrazination of Carbonyl Derivatives in Aqueous Media or in a Ball-Mill

Pyrrolidine-derived organocatalysts have been tested in two types of α-heterofunctionalization reactions in aqueous media or under solvent-free ball-milling conditions. The best results in terms of both activity and enantioselectivity were obtained with O

Heterogeneous Dipeptide-Catalyzed α-Amination of Aldehydes in a Continuous-Flow Reactor: Effect of Residence Time on Enantioselectivity

A solid-supported dipeptide-catalyzed continuous-flow process was developed for the direct enantioselective α-amination of aldehydes with dibenzyl azodicarboxylate as the electrophilic nitrogen source. With residence time control as an efficient tool for

Remarkable reaction rate and excellent enantioselective direct α-amination of aldehydes with azodicarboxylates catalyzed by pyrrolidinylcamphor-derived organocatalysts

Remarkable reaction rate and excellent enantioselective direct α-amination of unmodified aldehydes with various azodicarboxylates was catalyzed by pyrrolidinylcamphor organocatalyst 2a (5 mol-%) to provide the desired aminated products with excellent chemical yields and high to excellent levels of enantioselectivity (up to >99%ee) at 0 °C in CH 2Cl2.