890041-18-6

Basic information

• Product Name: N-[3-(N-tert-butoxycarbonyl-hydrazino)-phenyl]-hydrazinecarboxylic acid tert-butyl ester
• Synonyms: N-[3-(N-tert-butoxycarbonyl-hydrazino)-phenyl]-hydrazinecarboxylic acid tert-butyl ester
• CAS NO: 890041-18-6
• Molecular Weight: 338.407
• Mol File: 890041-18-6.mol

Chemical Properties

• CAS DataBase Reference: N-[3-(N-tert-butoxycarbonyl-hydrazino)-phenyl]-hydrazinecarboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-[3-(N-tert-butoxycarbonyl-hydrazino)-phenyl]-hydrazinecarboxylic acid tert-butyl ester(890041-18-6)
• EPA Substance Registry System: N-[3-(N-tert-butoxycarbonyl-hydrazino)-phenyl]-hydrazinecarboxylic acid tert-butyl ester(890041-18-6)

Safety Data

• Hazardous Substances Data: 890041-18-6(Hazardous Substances Data)

Upstream product

• 870-46-2 t-butoxycarbonylhydrazine 
• 626-00-6 1,3-Diiodobenzene 

Downstream Products

• 890041-20-0 di-tert-butyl 1,1'-(1,3-phenylene)bis(2-phenylhydrazinecarboxylate) 
• 890041-22-2 di-tert-butyl 1,1'-(1,3-phenylene)bis(2-(2,6-dimethylphenyl)hydrazinecarboxylate) 
• 890041-21-1 di-tert-butyl 1,1'-(1,3-phenylene)bis(2-o-tolylhydrazinecarboxylate) 

Relevant articles and documents

Synthesis and Structure of Functionalized Homo Heteracalix[2]arene[2]triazines: Effect of All Heteroatom Bridges on Macrocyclic Conformation

A number of unprecedented homo heteracalix[2]arene[2]triazines were synthesized by means of a fragment coupling approach. Two directional nucleophilic substitution reactions of N-Boc-protected 1,3-dihydrazobenzene with cyanuric acid chloride and 2-butoxy-

Regioselective [5,5]-sigmatropic rearrangement reactions of aryl hydrazides

N,N′-Aryl hydrazides with substituents at the ortho or meta positions undergo highly regioselective [5,5]-sigmatropic rearrangement reactions to furnish benzidines in good to excellent isolated yields. The presence of single substituent at either the ortho or meta position provides sufficient bias, effectively suppressing the formation of diphenylene, the major byproduct of the conventional benzidine rearrangement reaction.