1,2-Diphenylbenzimidazole

Base Information

Chemical Name:1,2-Diphenylbenzimidazole
CAS No.:2622-67-5
Molecular Formula:C19H14N2
Molecular Weight:270.334
Hs Code.:2933990090
NSC Number:99050
DSSTox Substance ID:DTXSID90180860
Nikkaji Number:J112.446C
Wikidata:Q72473052
Mol file:2622-67-5.mol

Synonyms:2622-67-5;1,2-diphenyl-1H-benzo[d]imidazole;1,2-Diphenylbenzimidazole;1,2-Diphenyl-1H-benzimidazole;1H-Benzimidazole, 1,2-diphenyl-;1,2-diphenyl-1H-benzoimidazole;Benzimidazole, 1,2-diphenyl-;1,2-diphenyl-1H-1,3-benzodiazole;NSC99050;Benzimidazole,2-diphenyl-;1,2-diphenyl-benzoimidazole;SCHEMBL541157;1H-Benzimidazole,2-diphenyl-;DTXSID90180860;1,2-Diphenyl-1H-benzimidazole #;MFCD00416995;NSC 99050;NSC-99050;AKOS002321222;BS-51569;A5210;CS-0156362;FT-0659210;D83170;A818331;2-([(4-METHOXYPHENYL)SULFONYL]AMINO)-3-PHENYLPROPANOICACID

Suppliers and Price of 1,2-Diphenylbenzimidazole

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

Matrix Scientific
1,2-Diphenyl-1H-benzo[d]imidazole 95+%
5g
$ 756.00

Matrix Scientific
1,2-Diphenyl-1H-benzo[d]imidazole 95+%
1g
$ 284.00

Crysdot
1,2-Diphenyl-1H-benzo[d]imidazole 95+%
5g
$ 353.00

Chemenu
1,2-Diphenyl-1H-benzo[d]imidazole 95%
5g
$ 333.00

American Custom Chemicals Corporation
1,2-DIPHENYL-1H-BENZIMIDAZOLE 95.00%
5G
$ 909.56

Alichem
1,2-Diphenyl-1H-benzo[d]imidazole
5g
$ 400.00

AK Scientific
1,2-Diphenyl-1H-benzimidazole
5g
$ 1070.00

Aaron Chemicals
1H-Benzimidazole,1,2-diphenyl- 95%
250mg
$ 59.00

Total 47 raw suppliers

Chemical Property of 1,2-Diphenylbenzimidazole

Chemical Property:

Vapor Pressure:5.92E-09mmHg at 25°C
Melting Point:111 °C
Refractive Index:1.644
Boiling Point:468.569 °C at 760 mmHg
PKA:4.16±0.10(Predicted)
Flash Point:237.182 °C
PSA：17.82000
Density:1.127 g/cm³
LogP:4.69250
Storage Temp.:Inert atmosphere,Room Temperature
XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:270.115698455
Heavy Atom Count:21
Complexity:331

Purity/Quality:

99%, ^*data from raw suppliers

1,2-Diphenyl-1H-benzo[d]imidazole 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC3=CC=CC=C3N2C4=CC=CC=C4
General Description 1,2-Diphenyl-1H-benzimidazole (Hpbi) is a ligand used in the synthesis of hetero-triplet iridium complexes, such as [Ir(ppy)₂pbi], where it contributes to the study of triplet-triplet annihilation and phosphorescent OLED performance. Additionally, it serves as a phenylbenzoimidazole-based cyclometalating ligand in cationic iridium(III) complexes, influencing their photophysical and electrochemical properties, as well as enhancing luminescence and stability.

Technology Process of 1,2-Diphenylbenzimidazole

There total 98 articles about 1,2-Diphenylbenzimidazole 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: 99.0%

: 100-46-9
benzylamine

: 534-85-0
N-phenyl-1,2-benzenediamine

: 2622-67-5
1,2-diphenyl-1H-benzoimidazole

Guidance literature:: With 4-tert-butyl-5-methoxy-1,2-benzoquinone; oxygen; toluene-4-sulfonic acid; In acetonitrile; at 60 ℃; for 24h; Schlenk technique;
DOI:10.1021/acs.orglett.7b02786

Reference yield: 99.0%

: 1527-91-9
N-phenylbenzamidine

: 583-53-9
2,3-dibromobenzene

: 2622-67-5
1,2-diphenyl-1H-benzoimidazole

Guidance literature:: With palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; sodium t-butanolate; In toluene; at 140 ℃; for 24h; regiospecific reaction; Molecular sieve; Inert atmosphere;
DOI:10.1021/ol202807d