138206-93-6

Basic information

• Product Name: dibenzyl 1-(1,2,3,4-tetrahydro-7-methoxy-1-oxo-2-naphthyl)-1,2-hydrazinedicarboxylate
• Synonyms: dibenzyl 1-(1,2,3,4-tetrahydro-7-methoxy-1-oxo-2-naphthyl)-1,2-hydrazinedicarboxylate
• CAS NO: 138206-93-6
• Molecular Weight: 474.513
• Mol File: 138206-93-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: dibenzyl 1-(1,2,3,4-tetrahydro-7-methoxy-1-oxo-2-naphthyl)-1,2-hydrazinedicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dibenzyl 1-(1,2,3,4-tetrahydro-7-methoxy-1-oxo-2-naphthyl)-1,2-hydrazinedicarboxylate(138206-93-6)
• EPA Substance Registry System: dibenzyl 1-(1,2,3,4-tetrahydro-7-methoxy-1-oxo-2-naphthyl)-1,2-hydrazinedicarboxylate(138206-93-6)

Safety Data

• Hazardous Substances Data: 138206-93-6(Hazardous Substances Data)

Upstream product

• 6836-19-7 7-Methoxy-1-tetralone 
• 2449-05-0 dibenzyl azodicarboxylate 

Downstream Products

• 138206-90-3 benzyl (3aRS,9bSR)-N-(2,3,3a,4,5,9b-hexahydro-8-methoxy-2-oxonaphth<2.1-d>oxazol-3-yl)carbamate 
• 138408-16-9 dibenzyl 1-<(1RS,2RS)-1,2,3,4-tetrahydro-1-hydroxy-7-methoxy-2-naphthyl>1,2-hydrazinedicarboxylate 
• 138206-95-8 dibenzyl 1-<(1RS,2SR)-1,2,3,4-tetrahydro-1-hydroxy-7-methoxy-2-naphthyl>-1,2-hydrazinedicarboxylate 
• 138206-95-8 C₂₇H₂₈N₂O₆ 
• 138206-97-0 (1,2,3,4-tetrahydro-7-methoxy-2-naphthyl)hydrazine 
• 4003-89-8 2-amino-7-methoxy-1,2,3,4-tetrahydronaphthalene 

Relevant articles and documents

Efficient Methodology for the Preparation of β-Aminotetralin Derivatives via Electrophilic Amination

A mild and efficient method for the construction of β-aryl amines from the corresponding α-aryl ketones is presented.The key step of the synthesis involve an electrophilic amination by dibenzyl azodicarboxylate followed by a stereoselective LiHBEt3 reduction.The reaction sequence is applied to the synthesis of the tricyclic ergoline analogue 4. Key words: electrophilic amination; stereoselective reduction; α-amino ketones.