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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Pyrazole-4-carbonitrile, 1-(1,1-dimethylethyl)-

N#Cc1cnn(c1)C(C)(C)C Request for Quotation
Chemical Name: 1H-Pyrazole-4-carbonitrile, 1-(1,1-dimethylethyl)-
CAS Number: 149139-43-5
Product Number: AG001LF8(AGN-PC-0NDF45)
Synonyms:
MDL No:
Molecular Formula: C8H11N3
Molecular Weight: 149.1930

Identification/Properties

Computed Properties
Molecular Weight:
149.197g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
149.095g/mol
Monoisotopic Mass:
149.095g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
183
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(tert-Butyl)-1H-pyrazole-4-carbonitrile, commonly known as $name$, is a versatile chemical compound that finds wide applications in chemical synthesis. This compound serves as a valuable building block in organic chemistry due to its unique structure and reactivity.$name$ is commonly used as a precursor in the synthesis of various bioactive compounds and pharmaceutical intermediates. Its carbonitrile group provides a valuable handle for further derivatization, allowing chemists to introduce a wide range of functional groups for the synthesis of complex molecules.In addition, $name$ can be utilized as a key starting material in the preparation of heterocyclic compounds, which are essential in drug discovery and development. Its pyrazole ring structure offers opportunities for the creation of diverse molecules with potential biological activities.Furthermore, $name$ can be employed in the synthesis of agrochemicals, dyes, and materials science applications. Its tert-butyl group and pyrazole core contribute to the stability and structural diversity of the resulting products, making it a valuable asset in the toolbox of synthetic chemists.Overall, the strategic incorporation of 1-(tert-Butyl)-1H-pyrazole-4-carbonitrile in chemical synthesis enables the efficient construction of intricate molecules with diverse functionalities, making it a highly sought-after compound in the field of organic chemistry.