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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)-1H-pyrrolo[3,2-b]pyridine

FC(c1cnc2c(c1)[nH]cc2)(F)F Request for Quotation
Chemical Name: 6-(trifluoromethyl)-1H-pyrrolo[3,2-b]pyridine
CAS Number: 1190311-44-4
Product Number: AG000HHA(AGN-PC-07ZRTE)
Synonyms:
MDL No:
Molecular Formula: C8H5F3N2
Molecular Weight: 186.1339

Identification/Properties

Properties
BP:
271°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
186.137g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
186.04g/mol
Monoisotopic Mass:
186.04g/mol
Topological Polar Surface Area:
28.7A^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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(Trifluoromethyl)-1H-pyrrolo[3,2-b]pyridine is a versatile building block in chemical synthesis due to its unique structural properties and reactivity. As a heterocyclic compound containing a trifluoromethyl group, this molecule serves as an important intermediate for the synthesis of various biologically active compounds, pharmaceuticals, agrochemicals, and materials. Its presence can influence the electronic and steric properties of the resulting molecules, making it a valuable tool in designing new compounds with desired properties. In organic synthesis, this compound can participate in diverse reactions, such as cross-coupling, cycloaddition, and functional group transformations, leading to the efficient construction of complex molecular scaffolds. Additionally, the trifluoromethyl group can enhance the metabolic stability and bioavailability of drug candidates, making this compound valuable in medicinal chemistry research. Its application spans across the fields of drug discovery, material science, and chemical biology, highlighting its significance in modern synthetic chemistry.