1H-Pyrazole-3-carboxylic acid, 4,5-dihydro-5-oxo-1-phenyl-4-(phenylazo)-, ethyl ester

Base Information

Chemical Name:1H-Pyrazole-3-carboxylic acid, 4,5-dihydro-5-oxo-1-phenyl-4-(phenylazo)-, ethyl ester
CAS No.:1914-78-9
Molecular Formula:C18H16N4O3
Molecular Weight:336.3446
Hs Code.:
DSSTox Substance ID:DTXSID60883770
Nikkaji Number:J1.394.296J
Mol file:1914-78-9.mol

Synonyms:1914-78-9;1H-Pyrazole-3-carboxylic acid, 4,5-dihydro-5-oxo-1-phenyl-4-(phenylazo)-, ethyl ester;1H-Pyrazole-3-carboxylic acid, 4,5-dihydro-5-oxo-1-phenyl-4-(2-phenyldiazenyl)-, ethyl ester;Ethyl 5-oxo-1-phenyl-4-phenylazo-2-pyrazoline-3-carboxylate;DTXSID60883770;Ethyl 5-oxo-1-phenyl-4-[(E)-phenyldiazenyl]-4,5-dihydro-1H-pyrazole-3-carboxylate #

Suppliers and Price of 1H-Pyrazole-3-carboxylic acid, 4,5-dihydro-5-oxo-1-phenyl-4-(phenylazo)-, ethyl ester

Supply Marketing:

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

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Chemical Property of 1H-Pyrazole-3-carboxylic acid, 4,5-dihydro-5-oxo-1-phenyl-4-(phenylazo)-, ethyl ester

Chemical Property:

Vapor Pressure:1.03E-08mmHg at 25°C
Boiling Point:461.9°Cat760mmHg
Flash Point:233.2°C
Density:1.28g/cm³
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:6
Exact Mass:336.12224039
Heavy Atom Count:25
Complexity:549

Purity/Quality:

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MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=NN(C(=O)C1N=NC2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 1H-Pyrazole-3-carboxylic acid, 4,5-dihydro-5-oxo-1-phenyl-4-(phenylazo)-, ethyl ester

There total 1 articles about 1H-Pyrazole-3-carboxylic acid, 4,5-dihydro-5-oxo-1-phenyl-4-(phenylazo)-, ethyl ester 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: