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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-iodo-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine

FC(c1cnc2c(c1)c(I)c[nH]2)(F)F Request for Quotation
Chemical Name: 3-iodo-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine
CAS Number: 1142192-57-1
Product Number: AG000AUL(AGN-PC-07XSM4)
Synonyms:
MDL No:
Molecular Formula: C8H4F3IN2
Molecular Weight: 312.0304

Identification/Properties

Computed Properties
Molecular Weight:
312.034g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
311.937g/mol
Monoisotopic Mass:
311.937g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
221
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:
Danger
UN#:
2811
Hazard Statements:
H301
Precautionary Statements:
P301+P310
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3-Iodo-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine is a versatile building block in chemical synthesis. It is commonly utilized in the pharmaceutical and agrochemical industries to synthesize biologically active compounds and new materials. With its unique structure and reactivity, this compound is particularly valuable in the formation of heterocyclic compounds and the introduction of fluorine-containing groups into organic molecules. Its ability to serve as a versatile intermediate in the preparation of complex molecules makes it a favored choice for medicinal chemists and synthetic organic chemists.