41002-34-0

Basic information

• Product Name: Benzenamine, 4-hydrazino-N,N-dimethyl-
• Synonyms: Benzenamine, 4-hydrazino-N,N-dimethyl-;4-hydrazinyl-N,N-dimethylbenzenamine
• CAS NO: 41002-34-0
• Molecular Formula: C₈H₁₃N₃
• Molecular Weight: 151.20892
• Mol File: 41002-34-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 102-104 °C
• Boiling Point: 303.2±25.0 °C(Predicted)
• Appearance: /
• Density: 1.127±0.06 g/cm3(Predicted)
• PKA: 7.41±0.24(Predicted)
• CAS DataBase Reference: Benzenamine, 4-hydrazino-N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-hydrazino-N,N-dimethyl-(41002-34-0)
• EPA Substance Registry System: Benzenamine, 4-hydrazino-N,N-dimethyl-(41002-34-0)

Safety Data

• Hazardous Substances Data: 41002-34-0(Hazardous Substances Data)

Upstream product

• 24564-52-1 4-(dimethylamino)benzenediazonium tetrafluoroborate 

Downstream Products

• 58-15-1 2-(4-dimethylamino-phenyl)-1,5-dimethyl-1,2-dihydro-pyrazol-3-one 

Relevant articles and documents

Reduction electrochimique des sels d'aryldiazonium en milieu aqueux: II. Effet de substituants sur la stabilisation du radical libre intermediaire de reduction et sur le rendement de la synthese d'arylhydrazines primaires

The polarographic behaviour of a series of aromatic diazonium salts , BF4- in aqueous media is reported and discussed.The half-wave potentials corresponding to the first reduction step have been correlated to Hammett substituent constant ? and are defined by the equation : E=0.14?-0.015+/-0.01 V vs SCE.Substituent effects on the yield of electrochemical synthesis on a mercury pool of by electrochemical reduction of aryldiazoniums salts 10E-3 mol.l-1 at 0 1,1 V vs.SCE are also investigated at low temperature.The best yield (70percent) are obtained with the electron donating substituents on the phenyl ring.Unfortunately, large scale electrolytic reduction of aromatic diazoniums 10E-2 mol.l-1 at -1,1 V vs SCE results in the formation of primary hydrazines in poor yields.On such a large scale, it no longer seems possible to minimize the competitive chemical side reactions.