14996-70-4

Basic information

• Product Name: 1,2-dimethyl-1,2-diphenylhydrazine
• Synonyms: Hydrazine, 1,2-dimethyl-1,2-diphenyl-
• CAS NO: 14996-70-4
• Molecular Formula: C₁₄H₁₆N₂
• Molecular Weight: 212.2902
• Mol File: 14996-70-4.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 303.4°C at 760 mmHg
• Flash Point: 124.9°C
• Density: 1.098g/cm³
• Vapor Pressure: 0.000931mmHg at 25°C
• Refractive Index: 1.642
• CAS DataBase Reference: 1,2-dimethyl-1,2-diphenylhydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-dimethyl-1,2-diphenylhydrazine(14996-70-4)
• EPA Substance Registry System: 1,2-dimethyl-1,2-diphenylhydrazine(14996-70-4)

Safety Data

• Hazardous Substances Data: 14996-70-4(Hazardous Substances Data)

Usage

Type of Compound

Hydrazine derivative and substituted hydrazine

Primary Use

Building block in the synthesis of pharmaceuticals and other organic compounds

Application

Production of various drugs and agrochemicals

Research Potential

Potential treatment for certain cancers

Toxicity

Toxic and poses health hazards

Safety Precautions

Proper safety measures should be taken when handling or working with this compound

Upstream product

• 122-66-7 diphenyl hydrazine 
• 74-88-4 methyl iodide 
• 1227476-15-4 Azobenzene 
• 110-71-4 1,2-dimethoxyethane 
• 17082-12-1 trans-azobenzene 
• 7664-41-7 ammonia 
• 100-61-8 N-methylaniline 
• 69-72-7 salicylic acid 
• 66168-29-4 N-methyl-N,S-diphenylthiohydroxylamine 
• 81413-31-2 α-N-methylanilino-γ-butyrolactone 
• 5579-27-1 1,4-dimethyl-1,4-diphenyl-2-tetrazine 
• 56-23-5 tetrachloromethane 
• 121-69-7 N,N-dimethyl-aniline 
• 917-54-4 methyllithium 

Downstream Products

• 100-61-8 N-methylaniline 
• 614-00-6 N-methyl-N-nitrosoaniline 
• 366-29-0 N,N,N',N'-tetramethylbenzidine 

Relevant articles and documents

CuCl-catalyzed Oxidative Coupling Reaction of Secondary Amines with Molecular Oxygen in Pyridine

Oxidation of diphenylamine with molecular oxygen in the presence of CuCl in pyridine at room temperature to give tetraphenylhydrazine in a high yield was achieved by selecting suitable reaction conditions.N-methylaniline was also oxidized to give N,N'-dim

Method for realizing N-N coupling of secondary arylamine by utilizing electrochemical reaction

The invention relates to the technical field of organic synthesis, and discloses a method for realizing the N-N coupling of secondary arylamine by utilizing electrochemical reaction, i.e., in a deviceprovided with an anode and a cathode, an Nmethylaniline

Chemoselective deprotonative lithiation of azobenzenes: Reactions and mechanisms

Whereas standard strong bases (n-BuLi, s-BuLi/TMEDA, n-BuLi/t-BuOK, TMPMgCl·LiCl, and LDA) reduce the N=N bond of the parent azobenzene (Y = H), aromatic H→Li permutation occurs with LTMP when a suitable director of lithiation (Y = OMe, CONEt2, F) is present in the benzene residue of the azo compound. The method allows direct access to new substituted azobenzenes.