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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)-

2(1H)-Pyridinone, 5-nitro-3-(trifluoromethyl)-

[O-][N+](=O)c1cnc(c(c1)C(F)(F)F)O Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 5-nitro-3-(trifluoromethyl)-
CAS Number: 99368-66-8
Product Number: AG00IK9W(AGN-PC-0KKWMH)
Synonyms:
MDL No:
Molecular Formula: C6H3F3N2O3
Molecular Weight: 208.0948

Identification/Properties

Computed Properties
Molecular Weight:
208.096g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
208.01g/mol
Monoisotopic Mass:
208.01g/mol
Topological Polar Surface Area:
74.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
350
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


5-Nitro-3-(trifluoromethyl)pyridin-2-ol is a versatile compound commonly used in chemical synthesis due to its unique chemical properties. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceutical agents. Its nitro group provides a reactive site for further functionalization through organic reactions such as reduction, nitration, or oxidation. The trifluoromethyl group enhances the compound's lipophilicity and can influence its pharmacokinetic properties. When incorporated into the chemical synthesis process, 5-Nitro-3-(trifluoromethyl)pyridin-2-ol can play a crucial role in the development of new materials, drug candidates, and agrochemicals. Its strategic placement within the molecular structure can lead to the formation of diverse molecules with enhanced biological activities or unique physical properties.