1-(4-Methoxyphenyl)-3-phenyl-1H-pyrazol-5-amine

Base Information

Chemical Name:1-(4-Methoxyphenyl)-3-phenyl-1H-pyrazol-5-amine
CAS No.:41554-51-2
Molecular Formula:C16H15N3O
Molecular Weight:265.315
Hs Code.:
European Community (EC) Number:622-204-4
Mol file:41554-51-2.mol

Synonyms:1-(4-METHOXYPHENYL)-3-PHENYL-1H-PYRAZOL-5-AMINE;41554-51-2;AKOS012474575;1-(4-METHOXYPHENYL)-3-PHENYL-1H-PYRAZOL-5-YLAMINE

Suppliers and Price of 1-(4-Methoxyphenyl)-3-phenyl-1H-pyrazol-5-amine

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

American Custom Chemicals Corporation
1-(4-METHOXYPHENYL)-3-PHENYL-1H-PYRAZOL-5-AMINE 95.00%
5G
$ 4244.63

American Custom Chemicals Corporation
1-(4-METHOXYPHENYL)-3-PHENYL-1H-PYRAZOL-5-AMINE 95.00%
1G
$ 1030.84

Total 1 raw suppliers

Chemical Property of 1-(4-Methoxyphenyl)-3-phenyl-1H-pyrazol-5-amine

Chemical Property:

PSA：53.07000
LogP:3.71130
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:265.121512110
Heavy Atom Count:20
Complexity:298

Purity/Quality:

99% ^*data from raw suppliers

1-(4-METHOXYPHENYL)-3-PHENYL-1H-PYRAZOL-5-AMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:COC1=CC=C(C=C1)N2C(=CC(=N2)C3=CC=CC=C3)N

Technology Process of 1-(4-Methoxyphenyl)-3-phenyl-1H-pyrazol-5-amine

There total 3 articles about 1-(4-Methoxyphenyl)-3-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:

: 93-89-0,99341-95-4
benzoic acid ethyl ester

: 41554-51-2
5-amino-1-(4-methoxylphenyl)-3-phenyl-1H-pyrazole

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium tert-butylate / tetrahydrofuran / 0.58 h / 17 - 19 °C

2.1: sulfuric acid / tetrahydrofuran / 0.08 h / 17 - 19 °C

2.2: 9 h / Reflux

With sulfuric acid; potassium tert-butylate; In tetrahydrofuran;
DOI:10.1039/c5cc02020d

Reference yield:

: 614-16-4
Benzoylacetonitrile

: 3471-32-7
4-Methoxyphenylhydrazine

: 41554-51-2
5-amino-1-(4-methoxylphenyl)-3-phenyl-1H-pyrazole

Guidance literature:: Benzoylacetonitrile; With sulfuric acid; In tetrahydrofuran; at 17 - 19 ℃; for 0.0833333h;

4-Methoxyphenylhydrazine; With hydrazine hydrate; In tetrahydrofuran; for 9h; regioselective reaction; Reflux;
DOI:10.1039/c5cc02020d