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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-Pyridinecarboxylic acid, 2-bromo-6-(trifluoromethyl)-

OC(=O)c1ccc(nc1Br)C(F)(F)F Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 2-bromo-6-(trifluoromethyl)-
CAS Number: 749875-07-8
Product Number: AG005RP4(AGN-PC-05C244)
Synonyms:
MDL No:
Molecular Formula: C7H3BrF3NO2
Molecular Weight: 270.0034

Identification/Properties

Properties
MP:
130-132 °C
BP:
289.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
270.005g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
268.93g/mol
Monoisotopic Mass:
268.93g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
234
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


2-Bromo-6-trifluoromethyl-3-pyridinecarboxylic acid is a versatile compound widely employed in chemical synthesis as a key building block. This compound serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure, featuring a trifluoromethyl group and a bromine atom on the pyridine ring, imparts specific reactivity that allows for the efficient construction of complex molecular architectures. In organic synthesis, 2-Bromo-6-trifluoromethyl-3-pyridinecarboxylic acid is utilized as a nucleophilic reagent, enabling the introduction of functional groups and facilitating the formation of carbon-carbon and carbon-heteroatom bonds. Its strategic incorporation into synthetic pathways contributes to the development of novel chemical entities with diverse applications and potential therapeutic benefits.