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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)-

1-[5-(trifluoromethyl)pyridin-2-yl]pyrazole-4-sulfonyl chloride

FC(c1ccc(nc1)n1ncc(c1)S(=O)(=O)Cl)(F)F Request for Quotation
Chemical Name: 1-[5-(trifluoromethyl)pyridin-2-yl]pyrazole-4-sulfonyl chloride
CAS Number: 1006441-36-6
Product Number: AG0002JU(AGN-PC-01XG3B)
Synonyms:
MDL No:
Molecular Formula: C9H5ClF3N3O2S
Molecular Weight: 311.6681

Identification/Properties

Computed Properties
Molecular Weight:
311.663g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
2
Exact Mass:
310.974g/mol
Monoisotopic Mass:
310.974g/mol
Topological Polar Surface Area:
73.2A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
425
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-(5-(Trifluoromethyl)pyridin-2-yl)-1H-pyrazole-4-sulfonyl chloride is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as a key building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 1-(5-(Trifluoromethyl)pyridin-2-yl)-1H-pyrazole-4-sulfonyl chloride is commonly used as a sulfonylating agent for introducing the sulfonyl group into various organic molecules. The presence of the sulfonyl chloride functional group confers unique reactivity and selectivity properties, making it a valuable tool for the modification of organic compounds.Additionally, this compound can participate in a variety of synthetic transformations such as nucleophilic substitution, palladium-catalyzed cross-coupling reactions, and metal-catalyzed functional group interconversions. Its reactivity profile makes it an indispensable reagent in the construction of complex molecular structures and the synthesis of bioactive compounds with potential therapeutic applications.