CAS 66751-32-4

6-Chloro-2,3-dihydro-1-(phenylmethyl)-1H-pyrrolo[3,2-c]pyridine-7-carbonitrile

Description:

6-Chloro-2,3-dihydro-1-(phenylmethyl)-1H-pyrrolo[3,2-c]pyridine-7-carbonitrile is a heterocyclic organic compound characterized by its complex structure, which includes a pyrrolopyridine framework. This compound features a chloro substituent and a carbonitrile group, contributing to its chemical reactivity and potential biological activity. The presence of the phenylmethyl group enhances its lipophilicity, which may influence its pharmacokinetic properties. Typically, compounds of this nature are investigated for their potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. The molecular structure suggests potential interactions with biological macromolecules, making it a candidate for further research in drug discovery. Additionally, the compound's stability, solubility, and reactivity can vary based on environmental conditions and the presence of other functional groups. Overall, 6-Chloro-2,3-dihydro-1-(phenylmethyl)-1H-pyrrolo[3,2-c]pyridine-7-carbonitrile represents a class of compounds that may exhibit significant therapeutic potential, warranting further investigation.

Formula: C₁₅H₁₂ClN₃

InChI: InChI=1S/C15H12ClN3/c16-15-13(8-17)14-12(9-18-15)6-7-19(14)10-11-4-2-1-3-5-11/h1-5,9H,6-7,10H2

InChI key: InChIKey=IVUBSTLZKRPWCD-UHFFFAOYSA-N

SMILES: C(N1C=2C(CC1)=CN=C(Cl)C2C#N)C3=CC=CC=C3

Synonyms:

• 1-Benzyl-6-chloro-1H,2H,3H-pyrrolo[3,2-c]pyridine-7-carbonitrile
• 1H-Pyrrolo[3,2-c]pyridine-7-carbonitrile, 6-chloro-2,3-dihydro-1-(phenylmethyl)-
• 6-Chloro-2,3-dihydro-1-(phenylmethyl)-1H-pyrrolo[3,2-c]pyridine-7-carbonitrile
• 1-Benzyl-6-chloro-2,3-dihydropyrrolo[3,2-c]pyridine-7-carbonitrile
• 1-Benzyl-6-chloro-7-cyano-5-azaindoline

1-Benzyl-6-chloro-1H,2H,3H-pyrrolo[3,2-c]pyridine-7-carbonitrile

CAS: 66751-32-4

1-Benzyl-6-chloro-1H,2H,3H-pyrrolo[3,2-c]pyridine-7-carbonitrile is an alkoxy compound that has been shown to react with amines and halogen to form pyridines. The compound also reacts with hydroxy groups and nucleophilic residues to form alkoxy groups. This reaction is catalyzed by hydroxy groups or a base such as sodium hydroxide or potassium hydroxide. 1-Benzyl-6-chloro-1H,2H,3H-pyrrolo[3,2-c]pyridine-7-carbonitrile can be used in the synthesis of polymers and plastics. It can also be used as a precursor for the synthesis of other compounds.

Formula: C₁₅H₁₂ClN₃

Purity: Min. 95%

Molecular weight: 269.73 g/mol

Ref: 3D-RCA75132