Diazene, phenyl(triphenylmethyl)-

Base Information

• Chemical Name: Diazene, phenyl(triphenylmethyl)-
• CAS No.: 981-18-0
• Molecular Formula: C25H20N2
• Molecular Weight: 348.447
• Hs Code.: 2927000090
• NSC Number: 36384
• UNII: EG76V425Q3
• DSSTox Substance ID: DTXSID7061358
• Nikkaji Number: J39.720B
• Mol file: 981-18-0.mol

Synonyms:1-Phenyl-2-trityldiazene;(Phenylazo)triphenylmethane;Diazene, phenyl(triphenylmethyl)-;Triphenylmethylazobenzene;Triphenyl(phenylazo)methane;981-18-0;Benzeneazomethane, 1',1',1'-triphenyl-;NSC 36384;NSC-36384;Diazene, 1-phenyl-2-(triphenylmethyl)-;NSC36384;phenylazotriphenylmethane;Phenyldiazotriphenylmethane;SCHEMBL491313;DTXSID7061358;(E)-phenyl(triphenylmethyl)diazene;EG76V425Q3;Benzeneazomethane,1',1'-triphenyl-;1-Phenyl-2-(triphenylmethyl)diazene;(1E)-1-Phenyl-2-(triphenylmethyl)diazene;Diazene, 1-phenyl-2-(triphenylmethyl)-, (1E)-

Chemical Property of Diazene, phenyl(triphenylmethyl)-

Chemical Property:

• Vapor Pressure: 3.72E-08mmHg at 25°C
• Boiling Point: 458.5°Cat760mmHg
• Flash Point: 223.9°C
• PSA: 24.72000
• Density: 1.03g/cm³
• LogP: 6.76240
• XLogP3: 6.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 348.162648646
• Heavy Atom Count: 27
• Complexity: 401

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)N=NC4=CC=CC=C4

Technology Process of Diazene, phenyl(triphenylmethyl)-

There total 9 articles about Diazene, phenyl(triphenylmethyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

N-phenyl-N'-triphenylmethylhydrazine (63418-38-2) → triphenyl(phenylazo)methane (981-18-0)

Guidance literature:

With carbon nanotube-rhodium nanohybrid; air; In chloroform; water; at 20 ℃; for 12h;

DOI:10.1039/c5cy00985e

Reference yield:

phenylhydrazine (100-63-0) → triphenyl(phenylazo)methane (981-18-0)

Guidance literature:

Multi-step reaction with 2 steps

1: absolute diethyl ether

2: diethyl ether; mixture of gaseous nitrogen oxides

With diethyl ether; mixture of gaseous nitrogen oxides;

Reference yield:

triphenylmethyl alcohol (76-84-6) + phenylhydrazine (100-63-0) → triphenyl(phenylazo)methane (981-18-0)

Guidance literature:

With acetic acid;

upstream raw materials:

triphenylmethyl alcohol

acetic acid

phenylhydrazine

N-phenyl-N'-triphenylmethylhydrazine

Downstream raw materials:

3-phenylpyridine

2-phenylpyridine

p-phenylpyridine

triphenylmethane