4-(1-Phenyl-1H-pyrazol-4-yl)benzenamine

Base Information

Chemical Name:4-(1-Phenyl-1H-pyrazol-4-yl)benzenamine
CAS No.:114474-29-2
Molecular Formula:C15H13N3
Molecular Weight:235.288
Hs Code.:
DSSTox Substance ID:DTXSID901279368
Mol file:114474-29-2.mol

Synonyms:4-(1-Phenyl-1H-pyrazol-4-yl)benzenamine;DTXSID901279368;AKOS005821006;114474-29-2

Suppliers and Price of 4-(1-Phenyl-1H-pyrazol-4-yl)benzenamine

Supply Marketing:

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

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Chemical Property of 4-(1-Phenyl-1H-pyrazol-4-yl)benzenamine

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:235.110947427
Heavy Atom Count:18
Complexity:255

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 4-(1-Phenyl-1H-pyrazol-4-yl)benzenamine

There total 3 articles about 4-(1-Phenyl-1H-pyrazol-4-yl)benzenamine 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: 82.0%

: 114474-27-0
1-Phenyl-4-(p-nitrophenyl)pyrazole

: 114474-29-2
1-Phenyl-4-(p-aminophenyl)pyrazole

Guidance literature:: With hydrogenchloride; tin(ll) chloride; In ethanol; for 3h; Heating;

Reference yield:

: 104-03-0
4-nitrobenzeneacetic acid

: 114474-29-2
1-Phenyl-4-(p-aminophenyl)pyrazole

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) POCl₃, 2.) 25 percent NaOH / 1.) 90 deg C, 6 h, 2.) 80 deg C to 85 deg C, 3 h

2: 80 percent / ethanol / 3 h / Heating

3: 82 percent / SnCl₂, HCl / ethanol / 3 h / Heating

With hydrogenchloride; sodium hydroxide; tin(ll) chloride; trichlorophosphate; In ethanol;

Reference yield:

: 93072-94-7
p-Nitrophenylmalondialdehyde

: 114474-29-2
1-Phenyl-4-(p-aminophenyl)pyrazole

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / ethanol / 3 h / Heating

2: 82 percent / SnCl₂, HCl / ethanol / 3 h / Heating

With hydrogenchloride; tin(ll) chloride; In ethanol;