ethyl 4-hydroxy-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate

Base Information

Chemical Name:ethyl 4-hydroxy-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate
CAS No.:26502-55-6
Molecular Formula:C₁₂H₁₁N₃O₅
Molecular Weight:277.236
Hs Code.:
DSSTox Substance ID:DTXSID601319886
ChEMBL ID:CHEMBL1595151
Mol file:26502-55-6.mol

Synonyms:ethyl 4-hydroxy-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate;26502-55-6;ethyl 4-hydroxy-1-(4-nitrophenyl)pyrazole-3-carboxylate;Oprea1_373610;MLS000775268;CHEMBL1595151;DTXSID601319886;HMS2770O11;AKOS001026478;SMR000368355;CS-0248226;EN300-39426;Z56778742;ethyl4-hydroxy-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate

Suppliers and Price of ethyl 4-hydroxy-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate

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
ETHYL 4-HYDROXY-1-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLATE 95.00%
5G
$ 1421.65

American Custom Chemicals Corporation
ETHYL 4-HYDROXY-1-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLATE 95.00%
2.5G
$ 1147.43

American Custom Chemicals Corporation
ETHYL 4-HYDROXY-1-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLATE 95.00%
1G
$ 808.89

Total 2 raw suppliers

Chemical Property of ethyl 4-hydroxy-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:277.06987046
Heavy Atom Count:20
Complexity:365

Purity/Quality:

99% ^*data from raw suppliers

ETHYL 4-HYDROXY-1-(4-NITROPHENYL)-1H-PYRAZOLE-3-CARBOXYLATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C1=NN(C=C1O)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of ethyl 4-hydroxy-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate

There total 5 articles about ethyl 4-hydroxy-1-(4-nitrophenyl)-1H-pyrazole-3-carboxylate 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: 77.0%

: [N-(3-Bromo-2-oxo-propyl)-N'-(4-nitro-phenyl)-hydrazino]-acetic acid ethyl ester

: 26502-55-6
ethyl 4-hydroxy-1-(p-nitrophenyl)pyrazole-3-carboxylate

Guidance literature:: With potassium acetate; In ethanol; for 0.166667h; Heating; other reagents: triethylamine, piperidine, morpholine, pyrrolidine other time: 2 h;