4-(1H-Benzimidazol-2-yl)-1-phenyl-1H-pyrazol-5-amine

Base Information

Chemical Name:4-(1H-Benzimidazol-2-yl)-1-phenyl-1H-pyrazol-5-amine
CAS No.:88105-10-6
Molecular Formula:C₁₆H₁₃N₅
Molecular Weight:275.313
Hs Code.:
DSSTox Substance ID:DTXSID00523087
Wikidata:Q82388896

Synonyms:88105-10-6;4-(1H-Benzimidazol-2-yl)-1-phenyl-1H-pyrazol-5-amine;DTXSID00523087;AKOS000181352

Suppliers and Price of 4-(1H-Benzimidazol-2-yl)-1-phenyl-1H-pyrazol-5-amine

Supply Marketing:

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

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Chemical Property of 4-(1H-Benzimidazol-2-yl)-1-phenyl-1H-pyrazol-5-amine

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:275.11709544
Heavy Atom Count:21
Complexity:357

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)N2C(=C(C=N2)C3=NC4=CC=CC=C4N3)N

Technology Process of 4-(1H-Benzimidazol-2-yl)-1-phenyl-1H-pyrazol-5-amine

There total 9 articles about 4-(1H-Benzimidazol-2-yl)-1-phenyl-1H-pyrazol-5-amine 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: 69.3%

: 88105-08-2,109385-61-7
3-amino-4-4--2-phenylpyrazole

: 88105-10-6
2-(5-Amino-1-phenylpyrazol-4-yl)benzimidazole

Guidance literature:: With hydrogenchloride; sodium carbonate; for 1h;

Reference yield: 17.0%

: 111828-30-9
1-Anilino-4-(2-aminoanilino)pyrimidin-2(1H)-one-5-carbonitrile

: 88105-10-6
2-(5-Amino-1-phenylpyrazol-4-yl)benzimidazole

: 111828-38-7
2-Anilinopyrimidino<1,6-a>benzimidazol-1(2H)-one-4-carbonitrile

Guidance literature:: With toluene-4-sulfonic acid; In ethanol; for 2.5h; Heating;

Reference yield:

: 42510-46-3
4-amino-1H-1,5-benzodiazepine-3-carbonitrile hydrochloride

: 88105-10-6
2-(5-Amino-1-phenylpyrazol-4-yl)benzimidazole

Guidance literature:: Multi-step reaction with 3 steps

1: 90.9 percent / H₂O / 2 h

2: 80 percent / NaOH / H₂O / 2.5 h / Heating

3: 69.3 percent / 1percent HCl, 10percent sodium carbonate / 1 h

With hydrogenchloride; sodium hydroxide; sodium carbonate; In water;