1H-Pyrrolo[2,3-b]pyridine-3-carbonitrile


Chemical Name: 1H-Pyrrolo[2,3-b]pyridine-3-carbonitrile
CAS Number: 4414-89-5
Product Number: AG003EEV(AGN-PC-0N2DUP)
Synonyms:
MDL No:
Molecular Formula: C8H5N3
Molecular Weight: 143.1454

Identification/Properties


Properties
MP:
258-262 °C
BP:
373.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
143.149g/mol
XLogP3:
1
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#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



1H-Pyrrolo[2,3-b]pyridine-3-carbonitrile, often referred to as $name$, is a key chemical intermediate widely used in chemical synthesis processes. This compound serves as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and functional materials due to its unique structural properties and reactivity.In organic chemistry, $name$ is involved in the construction of complex molecules through the formation of new carbon-carbon and carbon-nitrogen bonds. Its nitrile group provides the possibility for further functionalization, allowing for the introduction of different functional groups at specific positions on the molecule. This versatility makes $name$ a valuable tool in the synthesis of diverse chemical compounds.Moreover, the fused pyrrolopyridine ring system in $name$ offers opportunities for molecular diversity and conformational control in drug discovery and development. The presence of this heterocyclic motif is often associated with biological activity, making derivatives of $name$ attractive candidates for pharmaceutical research.Overall, the application of 1H-Pyrrolo[2,3-b]pyridine-3-carbonitrile in chemical synthesis is instrumental in the creation of novel molecules with potential use in various industries, highlighting its significance as a crucial building block in the synthesis of complex organic compounds.