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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-(3-pyridinyl)-

c1ccc(cn1)c1cnc2c(c1)cc[nH]2 Request for Quotation
Chemical Name: 1H-Pyrrolo[2,3-b]pyridine, 5-(3-pyridinyl)-
CAS Number: 918511-92-9
Product Number: AG00IGWR(AGN-PC-093R1U)
Synonyms:
MDL No:
Molecular Formula: C12H9N3
Molecular Weight: 195.2200

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
195.225g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
195.08g/mol
Monoisotopic Mass:
195.08g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
219
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(Pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridine is a versatile compound that serves as a valuable building block in chemical synthesis. Its unique structure and functional groups make it a key intermediate in the creation of various pharmaceuticals, agrochemicals, and materials.This compound is particularly useful in the development of heterocyclic compounds and complex organic molecules due to its ability to participate in a range of chemical reactions. It can undergo substitution, oxidation, reduction, and other transformations, allowing for the efficient and targeted synthesis of diverse products.In medicinal chemistry, 5-(Pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridine is utilized in the construction of drug candidates and bioactive molecules. Its presence in the molecular structure can enhance biological activity, improve pharmacokinetic properties, or modulate target selectivity, making it a valuable tool for drug discovery and development.Overall, the application of 5-(Pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridine in chemical synthesis enables researchers to access a wide range of functionalized compounds with tailored properties, paving the way for advancements in drug design, material science, and organic chemistry.