1-ethyl-1H-pyrazole-3-carbonitrile

Base Information

Chemical Name:1-ethyl-1H-pyrazole-3-carbonitrile
CAS No.:1006471-40-4
Molecular Formula:C₆H₇N₃
Molecular Weight:121.142
Hs Code.:2933199090
European Community (EC) Number:890-060-1
DSSTox Substance ID:DTXSID00599121
Wikidata:Q82494975
Mol file:1006471-40-4.mol

Synonyms:1-ethyl-1H-pyrazole-3-carbonitrile;1006471-40-4;1-ethylpyrazole-3-carbonitrile;SCHEMBL15096488;DTXSID00599121;BBL039934;MFCD04969701;STK349583;AKOS000309991;LS-04398;DB-421584;CS-0298456;EN300-229462;1-ethyl-1H-pyrazole-3-carbonitrile(SALTDATA: FREE)

Suppliers and Price of 1-ethyl-1H-pyrazole-3-carbonitrile

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

TRC
1-Ethyl-1H-pyrazole-3-carbonitrile
500mg
$ 130.00

Matrix Scientific
1-Ethyl-1H-pyrazole-3-carbonitrile
500mg
$ 218.00

Crysdot
1-Ethyl-1H-pyrazole-3-carbonitrile 95+%
1g
$ 332.00

CHESS?
MC005064:1-Ethyl-1H-pyrazole-3-carbonitrile 95
5 g
$ 1440.00

Chemenu
1-Ethyl-1H-pyrazole-3-carbonitrile 95%
1g
$ 313.00

American Custom Chemicals Corporation
1-ETHYL-1H-PYRAZOLE-3-CARBONITRILE 95.00%
5MG
$ 504.43

AK Scientific
1-Ethyl-1H-pyrazole-3-carbonitrile
500mg
$ 344.00

Total 8 raw suppliers

Chemical Property of 1-ethyl-1H-pyrazole-3-carbonitrile

Chemical Property:

PSA：41.61000
LogP:0.77468
XLogP3:0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:121.063997236
Heavy Atom Count:9
Complexity:135

Purity/Quality:

97% ^*data from raw suppliers

1-Ethyl-1H-pyrazole-3-carbonitrile ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN1C=CC(=N1)C#N

Technology Process of 1-ethyl-1H-pyrazole-3-carbonitrile

There total 1 articles about 1-ethyl-1H-pyrazole-3-carbonitrile 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:

: 75-03-6
ethyl iodide

: 36650-74-5
pyrazolecarbonitrile

: 1006471-40-4
1-ethyl-1H-pyrazole-3-carbonitrile

Guidance literature:: pyrazolecarbonitrile; With sodium hydride; In tetrahydrofuran; mineral oil; at 20 ℃; for 1h;

ethyl iodide; In tetrahydrofuran; mineral oil; at 20 ℃;

Reference yield:

: 1006471-40-4
1-ethyl-1H-pyrazole-3-carbonitrile

: 3-(((1-ethyl-1H-pyrazol-3-yl)methyl)amino)-2-nitrobenzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 20 °C / Cooling

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 20 °C

With lithium aluminium tetrahydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; N,N-dimethyl-formamide;

Reference yield:

: 1006471-40-4
1-ethyl-1H-pyrazole-3-carbonitrile

: (2-(6-((2S,5S)-2,5-dimethylpyrrolidin-1-yl)pyridin-3-yl)-1-((1-ethyl-1H-pyrazol-3-yl)methyl)-1H-benzo[d]imidazol-5-yl)boronic acid

Guidance literature:: Multi-step reaction with 4 steps

1: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 20 °C / Cooling

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 20 °C

3: sodium dithionite / water; ethanol / 0.33 h / 130 °C / Microwave irradiation

4: N-ethyl-N,N-diisopropylamine; 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); triphenylphosphine / ethanol / 16 h / 80 °C / Inert atmosphere

With lithium aluminium tetrahydride; sodium dithionite; 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; diethyl ether; ethanol; water; N,N-dimethyl-formamide;