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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)-

1H-Pyrrolo[2,3-b]pyridine, 5-fluoro-

Fc1cnc2c(c1)cc[nH]2 Request for Quotation
Chemical Name: 1H-Pyrrolo[2,3-b]pyridine, 5-fluoro-
CAS Number: 866319-00-8
Product Number: AG0036DE(AGN-PC-02ZNQM)
Synonyms:
MDL No:
Molecular Formula: C7H5FN2
Molecular Weight: 136.1264

Identification/Properties

Properties
MP:
110 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
136.129g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
136.044g/mol
Monoisotopic Mass:
136.044g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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#:
N/A
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Fluoro-1H-pyrrolo[2,3-b]pyridine is a versatile building block commonly used in chemical synthesis due to its unique structural features and reactivity. This compound serves as an important intermediate in the production of various pharmaceuticals, agrochemicals, and functional materials. Its substituted pyrrole and pyridine rings make it an ideal candidate for the synthesis of complex organic molecules through versatile reactions such as nucleophilic substitution, cycloaddition, and cross-coupling.One of the key applications of 5-Fluoro-1H-pyrrolo[2,3-b]pyridine is in medicinal chemistry, where it has been utilized in the development of novel drugs targeting various biological pathways. Its fluorine substitution provides enhanced lipophilicity and influences the compound's pharmacokinetic properties, making it valuable for structure-activity relationship studies and lead optimization in drug discovery.In addition, 5-Fluoro-1H-pyrrolo[2,3-b]pyridine plays a crucial role in the synthesis of functional materials with tailored properties, including optoelectronic materials, liquid crystals, and organic semiconductors. Its structural flexibility and ability to undergo diverse chemical transformations enable the creation of novel molecular architectures with specific electronic and optical functions.Overall, the use of 5-Fluoro-1H-pyrrolo[2,3-b]pyridine in chemical synthesis enables the rapid and efficient construction of complex molecules with diverse applications in the fields of pharmaceuticals, materials science, and agrochemicals.