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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-(difluoromethyl)-1-methylpyrazole-4-carboxamide

Cn1nc(c(c1)C(=O)N)C(F)F Request for Quotation
Chemical Name: 3-(difluoromethyl)-1-methylpyrazole-4-carboxamide
CAS Number: 925689-10-7
Product Number: AG0063WR(AGN-PC-0806V2)
Synonyms:
MDL No:
Molecular Formula: C6H7F2N3O
Molecular Weight: 175.1361

Identification/Properties

Computed Properties
Molecular Weight:
175.139g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
175.056g/mol
Monoisotopic Mass:
175.056g/mol
Topological Polar Surface Area:
60.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
188
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

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


1H-Pyrazole-4-carboxamide, 3-(difluoromethyl)-1-methyl- is a versatile compound that finds extensive application in chemical synthesis. Its unique chemical properties make it a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other organic compounds. With its difluoromethyl and methyl functional groups, this compound serves as a key intermediate in the synthesis of complex molecules.In organic synthesis, 1H-Pyrazole-4-carboxamide, 3-(difluoromethyl)-1-methyl- acts as a crucial starting material for the preparation of fluorinated heterocycles, which are essential in drug discovery and material science. The difluoromethyl group imparts distinct physicochemical properties to the resulting molecules, enhancing their biological activities and binding affinities.Furthermore, this compound can participate in various reactions such as nucleophilic substitutions, cross-coupling reactions, and cyclizations to introduce fluorinated motifs into organic structures. Its presence in the synthesis of biologically active compounds underscores its importance in medicinal chemistry research and development.Overall, 1H-Pyrazole-4-carboxamide, 3-(difluoromethyl)-1-methyl- serves as a valuable tool for chemists engaged in the design and production of novel compounds with enhanced properties and diverse functionalities in the field of chemical synthesis.