CAS 50781-87-8
:2,3-dihydro-1H-indol-1-ylacetonitrile
Description:
2,3-Dihydro-1H-indol-1-ylacetonitrile, with the CAS number 50781-87-8, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a nitrile functional group (-C≡N) attached to an acetic acid derivative, specifically at the 1-position of the indole. It is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. The presence of the nitrile group suggests potential reactivity, particularly in nucleophilic addition reactions. Additionally, the indole moiety is known for its biological significance, often serving as a scaffold in pharmaceuticals and natural products. The compound may exhibit various biological activities, although specific data on its pharmacological properties may be limited. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.
Formula:C10H10N2
InChI:InChI=1/C10H10N2/c11-6-8-12-7-5-9-3-1-2-4-10(9)12/h1-4H,5,7-8H2
SMILES:c1ccc2c(c1)CCN2CC#N
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
2-(2,3-Dihydro-1H-indol-1-yl)acetonitrile
CAS:<p>2-(2,3-Dihydro-1H-indol-1-yl)acetonitrile is a chemical with the molecular formula of C9H7N. It has a cyano group and stabilized carbanions. The compound is used in organic synthesis as a reagent to make various products, such as spiropyrans and perchlorate. It can also be transformed into indoline derivatives through condensation reactions with aromatic aldehydes.</p>Formula:C10H10N2Purity:Min. 95%Molecular weight:158.2 g/mol
