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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-(trifluoromethyl)imidazo[1,2-a]pyridine-8-carboxylic acid

OC(=O)c1cccn2c1nc(c2)C(F)(F)F Request for Quotation
Chemical Name: 2-(trifluoromethyl)imidazo[1,2-a]pyridine-8-carboxylic acid
CAS Number: 73221-20-2
Product Number: AG00FFBC(AGN-PC-0BHSDA)
Synonyms:
MDL No:
Molecular Formula: C9H5F3N2O2
Molecular Weight: 230.1434

Identification/Properties

Computed Properties
Molecular Weight:
230.146g/mol
XLogP3:
2.2
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


The 2-(Trifluoromethyl)imidazo[1,2-a]pyridine-8-carboxylic acid is a versatile compound widely utilized in chemical synthesis. This compound finds application as a key building block in the creation of pharmaceuticals, agrochemicals, and functional materials due to its unique structure and reactivity. When used in chemical synthesis, this compound serves as a valuable intermediate in the production of various heterocyclic compounds with diverse biological activities. Its trifluoromethyl group imparts enhanced physicochemical properties and biological activities to the final products, making it a valuable tool for medicinal chemists and material scientists alike.