N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine

Base Information

Chemical Name:N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine
CAS No.:133929-18-7
Molecular Formula:C₁₃H₁₂N₄
Molecular Weight:224.265
Hs Code.:
DSSTox Substance ID:DTXSID101327886
ChEMBL ID:CHEMBL1587003
Mol file:133929-18-7.mol

Synonyms:N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine;133929-18-7;4-N-(1H-benzimidazol-2-yl)benzene-1,4-diamine;N1-(1H-Benzo[d]imidazol-2-yl)benzene-1,4-diamine;MLS001208378;SMR000514583;N1-(1H-1,3-BENZODIAZOL-2-YL)BENZENE-1,4-DIAMINE;SR-01000325124;CHEMBL1587003;SCHEMBL20685416;DTXSID101327886;HMS2818G16;AKOS000301187;BB 0258278;CS-0233145;EN300-13113832;SR-01000325124-1;SR-01000325124-3;SR-01000325124-4

Suppliers and Price of N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine

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
N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine
1g
$ 308.00

Matrix Scientific
N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine
500mg
$ 200.00

Crysdot
N1-(1H-Benzo[d]imidazol-2-yl)benzene-1,4-diamine 97%
5g
$ 874.00

American Custom Chemicals Corporation
N-(1H-BENZOIMIDAZOL-2-YL)-BENZENE-1,4-DIAMINE 95.00%
500MG
$ 777.32

AK Scientific
N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine
5g
$ 1381.00

AK Scientific
N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine
2.5g
$ 966.00

Total 3 raw suppliers

Chemical Property of N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:224.106196400
Heavy Atom Count:17
Complexity:250

Purity/Quality:

98%min ^*data from raw suppliers

N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)NC3=CC=C(C=C3)N
Uses N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine can be used to fight emerging viruses.

Technology Process of N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine

There total 5 articles about N-(1H-Benzoimidazol-2-yl)-benzene-1,4-diamine 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: 68.0%

: 26946-70-3
N-(4-nitrophenyl)-1H-benzo[d]imidazol-2-amine

: 133929-18-7
2-(4-aminophenylamino)benzimidazole

Guidance literature:: With hydrogenchloride; tin; for 2h; Heating;

Reference yield:

: 615-16-7
1,3-dihydro-2H-benzimidazol-2-one

: 133929-18-7
2-(4-aminophenylamino)benzimidazole

Guidance literature:: Multi-step reaction with 2 steps

1: trichlorophosphate / 2 h / Reflux

2: 5,5-dimethyl-1,3-cyclohexadiene / 0.25 h / 200 °C / Microwave irradiation

With trichlorophosphate; In 5,5-dimethyl-1,3-cyclohexadiene;
DOI:10.1021/acsinfecdis.6b00202