N-(4-Cyano-1,3-diphenyl-1H-pyrazol-5-yl)-2-iodoacetamide

Base Information

Chemical Name:N-(4-Cyano-1,3-diphenyl-1H-pyrazol-5-yl)-2-iodoacetamide
CAS No.:189757-40-2
Molecular Formula:C18H13IN4O
Molecular Weight:428.232
Hs Code.:
DSSTox Substance ID:DTXSID80571384
Nikkaji Number:J815.655G
Wikidata:Q82459458
Mol file:189757-40-2.mol

Synonyms:189757-40-2;N-(4-Cyano-1,3-diphenyl-1H-pyrazol-5-yl)-2-iodoacetamide;DTXSID80571384

Suppliers and Price of N-(4-Cyano-1,3-diphenyl-1H-pyrazol-5-yl)-2-iodoacetamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-(4-Cyano-1,3-diphenyl-1H-pyrazol-5-yl)-2-iodoacetamide

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:428.01341
Heavy Atom Count:24
Complexity:479

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NN(C(=C2C#N)NC(=O)CI)C3=CC=CC=C3

Technology Process of N-(4-Cyano-1,3-diphenyl-1H-pyrazol-5-yl)-2-iodoacetamide

There total 2 articles about N-(4-Cyano-1,3-diphenyl-1H-pyrazol-5-yl)-2-iodoacetamide 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: 96.0%

: 189757-39-9
5-(chloroacetylamino)-1,3-diphenyl-1H-pyrazol-4-carbonitrile

: 189757-40-2
5-(iodo-acetylamino)-1,3-diphenyl-1H-pyrazol-4-carbonitrile

Guidance literature:: With potassium iodide; In acetone; for 3h; Heating;
DOI:10.3987/COM-96-7700

Reference yield:

: 5515-31-1
5-amino-1,3-diphenylpyrazole-4-carbonitrile

: 189757-40-2
5-(iodo-acetylamino)-1,3-diphenyl-1H-pyrazol-4-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: nitromethane / 0.75 h / Heating

2: 96 percent / potassium iodide / acetone / 3 h / Heating

With potassium iodide; In nitromethane; acetone;
DOI:10.3987/COM-96-7700