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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)-

5-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid

OC(=O)c1cn2c(n1)cccc2C(F)(F)F Request for Quotation
Chemical Name: 5-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid
CAS Number: 1260798-62-6
Product Number: AG000RBS(AGN-PC-0JF400)
Synonyms:
MDL No:
Molecular Formula: C9H5F3N2O2
Molecular Weight: 230.1434

Identification/Properties

Computed Properties
Molecular Weight:
230.146g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
230.03g/mol
Monoisotopic Mass:
230.03g/mol
Topological Polar Surface Area:
54.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
295
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


$Name$ is a versatile chemical compound that plays a crucial role in chemical synthesis processes. It is widely used as a key building block in the development of pharmaceuticals, agrochemicals, and advanced materials. The unique structure of 5-(Trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid imparts distinct properties that enhance the efficiency and specificity of various reactions.In chemical synthesis, $name$ serves as an important intermediate in the formation of diverse organic compounds. Its trifluoromethyl functional group not only provides steric and electronic effects but also improves the stability and reactivity of the resulting products. This makes it an ideal candidate for introducing fluorine-containing moieties into complex molecules, a crucial strategy in medicinal chemistry and materials science.Moreover, the imidazo[1,2-a]pyridine core of $name$ offers a versatile scaffold for further modifications, allowing chemists to tailor the compound for specific applications. By leveraging the unique reactivity and selectivity of this compound, researchers can efficiently access a wide range of structurally diverse molecules with potential biological activities or material properties.Overall, the strategic incorporation of 5-(Trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylic acid in chemical synthesis enables the synthesis of novel compounds with enhanced properties, making it a valuable tool for advancing research and innovation in various fields of chemistry.