1-Triazene, 1,3-bis(4-chlorophenyl)-

Base Information

Chemical Name:1-Triazene, 1,3-bis(4-chlorophenyl)-
CAS No.:3470-39-1
Molecular Formula:C12H9 Cl2 N3
Molecular Weight:266.13
Hs Code.:
NSC Number:85637
DSSTox Substance ID:DTXSID60292803
Nikkaji Number:J596.957C
ChEMBL ID:CHEMBL169687
Mol file:3470-39-1.mol

Synonyms:1-Triazene, 1,3-bis(4-chlorophenyl)-;3470-39-1;4,4'-Dichlorodiazoaminobenzene;1,3-Bis(p-chlorophenyl)triazene;1-Triazene, 1,3-bis[4-chlorophenyl]-;NSC85637;Triazene, 1,3-bis(p-chlorophenyl)-;4,4'-dichlordiazoaminobenzol;CBDivE_014158;CHEMBL169687;SCHEMBL24133218;DTXSID60292803;Triazene,3-bis(p-chlorophenyl)-;JGGKQOIDGHALJJ-UHFFFAOYSA-N;1-Triazene,3-bis(4-chlorophenyl)-;NSC-85637;STK695373;AKOS005606254;(1E)-1,3-bis(4-chlorophenyl)triaz-1-ene

Suppliers and Price of 1-Triazene, 1,3-bis(4-chlorophenyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of 1-Triazene, 1,3-bis(4-chlorophenyl)-

Chemical Property:

Vapor Pressure:1.21E-05mmHg at 25°C
Boiling Point:369.2°C at 760 mmHg
Flash Point:177.1°C
Density:1.32g/cm³
XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:265.0173527
Heavy Atom Count:17
Complexity:244

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1NN=NC2=CC=C(C=C2)Cl)Cl
General Description (1E)-1,3-bis(4-chlorophenyl)triaz-1-ene (1E)-1,3-bis(4-chlorophenyl)triaz-1-ene (also known as 1,3-bis(p-chlorophenyl)triazene) serves as a ligand in coordination chemistry, forming dinuclear palladium complexes such as **Pd₂L₄**, which exhibit electro-catalytic properties. Its structure has been confirmed by ¹H NMR and X-ray crystallography. While the diazo coupling mechanism of its precursor (p-chloroaniline) involves proton transfer and base catalysis, this specific triazene derivative's reactivity is primarily explored in metal complexation rather than its standalone chemical behavior.

Technology Process of 1-Triazene, 1,3-bis(4-chlorophenyl)-

There total 10 articles about 1-Triazene, 1,3-bis(4-chlorophenyl)- 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: 91.0%

: 106-47-8
4-chloro-aniline

: 3470-39-1
1,3-bis(p-chlorophenyl)triazene

Guidance literature:: With SHNC; In water; for 13h; Ambient temperature;
DOI:10.1021/jo9703820

Reference yield: 64.0%

: 106-47-8
4-chloro-aniline

: 2051-62-9,80333-62-6
4'-biphenyl chloride

: 3470-39-1
1,3-bis(p-chlorophenyl)triazene

Guidance literature:: With nitrogen(II) oxide; In benzene;
DOI:10.1016/00404-0399(50)1715T-

Reference yield:

: 106-47-8
4-chloro-aniline

: 110213-25-7,133611-12-8,77887-33-3
C₆H₄ClN₂O^(1-)*Na⁽¹⁺⁾

: 3470-39-1
1,3-bis(p-chlorophenyl)triazene

Guidance literature:: 4-chloro-aniline; With hydrogenchloride; sodium nitrite; In water; at 0 ℃; for 0.5h; Inert atmosphere;

With sodium hydroxide; In water; at 0 ℃; for 0.0833333h; Reagent/catalyst; Inert atmosphere;
DOI:10.1002/chem.201701429