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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)-

6-Trifluoromethyl-imidazo[1,2-a]pyridine

FC(c1ccc2n(c1)ccn2)(F)F Request for Quotation
Chemical Name: 6-Trifluoromethyl-imidazo[1,2-a]pyridine
CAS Number: 936009-02-8
Product Number: AG006EX3(AGN-PC-0WAC36)
Synonyms:
MDL No:
Molecular Formula: C8H5F3N2
Molecular Weight: 186.1339

Identification/Properties

Properties
MP:
98-99°
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
186.137g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
186.04g/mol
Monoisotopic Mass:
186.04g/mol
Topological Polar Surface Area:
17.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
192
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H317-H319
Precautionary Statements:
P280-P301+P312+P330-P305+P351+P338-P333+P313-P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(Trifluoromethyl)imidazo[1,2-a]pyridine is a versatile building block used in chemical synthesis to introduce a trifluoromethyl group into organic molecules. This compound serves as a valuable source of the trifluoromethyl functionality, which is known for its powerful influence on the physical and chemical properties of the resulting compounds. The presence of the trifluoromethyl group in organic molecules can enhance their biological activity, stability, and lipophilicity. In chemical synthesis, 6-(Trifluoromethyl)imidazo[1,2-a]pyridine can be utilized in the development of pharmaceuticals, agrochemicals, and materials. It offers a strategic approach to modify the structure of organic molecules, leading to the creation of new compounds with improved properties. This compound plays a crucial role in the construction of complex molecules and the discovery of novel chemical entities with potential applications in various fields.