1571-74-0

Basic information

• Product Name: 1,4-Benzenediamine, N,N'-bis(trimethylsilyl)-
• CAS NO: 1571-74-0
• Molecular Formula: C12H24N2Si2
• Molecular Weight: 252.507
• Mol File: 1571-74-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,4-Benzenediamine, N,N'-bis(trimethylsilyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Benzenediamine, N,N'-bis(trimethylsilyl)-(1571-74-0)
• EPA Substance Registry System: 1,4-Benzenediamine, N,N'-bis(trimethylsilyl)-(1571-74-0)

Safety Data

• Hazardous Substances Data: 1571-74-0(Hazardous Substances Data)

Usage

Chemical compound

Diaminobenzene derivative

Usage

Reagent in organic synthesis

Physical appearance

White to light yellow solid

Molecular weight

315.57 g/mol

Application

Preparation of trimethylsilyl-protected primary amines

Application

Precursor for the synthesis of various organic compounds

Potential application

Material science for silicon-containing polymers and materials

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 106-50-3 1,4-phenylenediamine 

Downstream Products

• 82765-03-5 p-Bis(trimethylsilyl)schwefel(IV)diimido-benzol 
• 249931-55-3 [(CH₃)2N]3ZrN[Si(CH₃)3]C₆H₄N[Si(CH₃)3]Zr[N(CH₃)2]3 
• 249931-57-5 C₁₂N₄Zr₂H₈[Si(CH₃)3]4[N(CH₃)2]4 
• 139041-55-7 C₆H₄(NWCl₄)2 
• 25811-68-1 N,N,N',N'-tetrakis(trimethylsilyl)-1,4-phenylenediamine 

Relevant articles and documents

Synthesis and application of some dianilinosilanes, bis (trimethylsilyl) phenylenediamines and dialkyl benzo-1,3,2-diazasilolines as antioxidants

A number of dialkyl or diphenyl dianilinosilanes, bis (trimethylsilyl) phenylenediamines and dialkyl benzo-1,3,2-diazasilolines were synthesized and used as antioxidants for lubricating base oils. Thermal analysis methods (DSC, TG and DTG) and IR techniqu

Structures of Sterically Overcrowded and Charge-Perturbed Molecules, 38. - The Different Conformations of N-Trimethylsilyl-Substituted p-Phenylenediamine Derivatives: Investigation of Single Crystals and in the Gas Phase

The ESR-proven generation of a Wurster's Blue radical anion by one-electron reduction of N,N,N',N'-tetrakis(trimethylsilyl)-p-phenylenediamine is rationalized by a posterior single-crystal structure determination of the neutral molecule, which demonstrate