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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[3,2-b]pyridine-6-carbonitrile

N#Cc1cnc2c(c1)[nH]cc2 Request for Quotation
Chemical Name: 1H-pyrrolo[3,2-b]pyridine-6-carbonitrile
CAS Number: 944937-79-5
Product Number: AG003N74(AGN-PC-04G0H9)
Synonyms:
MDL No:
Molecular Formula: C8H5N3
Molecular Weight: 143.1454

Identification/Properties

Properties
BP:
373°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
143.149g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
143.048g/mol
Monoisotopic Mass:
143.048g/mol
Topological Polar Surface Area:
52.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
193
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Pyrrolo[3,2-b]pyridine-6-carbonitrile is a versatile compound commonly utilized in chemical synthesis for the development of various pharmaceuticals, agrochemicals, and materials. This heterocyclic compound serves as a valuable building block in organic chemistry due to its unique structural features and reactivity.In chemical synthesis, 1H-Pyrrolo[3,2-b]pyridine-6-carbonitrile is often employed as a key intermediate in the preparation of biologically active compounds. Its incorporation into complex molecules allows for the introduction of specific functional groups and pharmacophores, enabling the modulation of desired biological activities. Additionally, the presence of the cyano group provides a convenient handle for further derivatization, facilitating the synthesis of structurally diverse compounds.Furthermore, the fused pyrrolopyridine ring system of 1H-Pyrrolo[3,2-b]pyridine-6-carbonitrile imparts desirable properties to the molecules it is incorporated into, such as improved pharmacokinetic profiles, enhanced binding affinity to biological targets, and increased molecular stability. This makes it a valuable scaffold for the design and synthesis of novel drug candidates and lead compounds in medicinal chemistry research.Overall, the utility of 1H-Pyrrolo[3,2-b]pyridine-6-carbonitrile in chemical synthesis lies in its ability to enable the efficient construction of diverse chemical structures with potential biological activity, making it an indispensable tool for drug discovery and materials science applications.