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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)-

3-nitro-1H-pyrazole-5-carbonitrile

N#Cc1[nH]nc(c1)[N+](=O)[O-] Request for Quotation
Chemical Name: 3-nitro-1H-pyrazole-5-carbonitrile
CAS Number: 1204246-72-9
Product Number: AG00HFGK(AGN-PC-0DA5Z0)
Synonyms:
MDL No:
Molecular Formula: C4H2N4O2
Molecular Weight: 138.08428

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Nitro-1H-pyrazole-5-carbonitrile is a versatile compound that finds wide application in chemical synthesis. This compound is commonly used as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structural properties, 3-Nitro-1H-pyrazole-5-carbonitrile serves as a valuable intermediate in the synthesis of biologically active molecules and other complex organic compounds.In chemical synthesis, 3-Nitro-1H-pyrazole-5-carbonitrile can undergo various reactions such as nucleophilic substitution, reduction, and cyclization to introduce different functional groups and structural motifs. These reactions allow chemists to modify the molecular structure of the compound, leading to the creation of novel derivatives with desired properties and activities.The presence of the nitro group in 3-Nitro-1H-pyrazole-5-carbonitrile also imparts unique reactivity, enabling selective transformations and functionalization. Moreover, the carbonitrile moiety offers opportunities for further derivatization through various synthetic pathways, facilitating the development of diverse chemical compounds for different applications.Overall, the utility of 3-Nitro-1H-pyrazole-5-carbonitrile in chemical synthesis lies in its ability to serve as a versatile building block for the construction of complex molecules with potential biological, agricultural, or industrial significance.