
CAS 132431-12-0
:Phenylmethyl 2,3-dihydro-1H-indole-1-carboxylate
Description:
Phenylmethyl 2,3-dihydro-1H-indole-1-carboxylate, identified by its CAS number 132431-12-0, 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 substance features a carboxylate functional group, contributing to its reactivity and potential applications in organic synthesis. The presence of the phenylmethyl group enhances its lipophilicity, which may influence its biological activity and solubility in organic solvents. Typically, compounds of this nature may exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The dihydro form indicates that the compound has undergone partial hydrogenation, which can affect its stability and reactivity. Overall, the unique structural features of Phenylmethyl 2,3-dihydro-1H-indole-1-carboxylate suggest potential utility in various chemical applications, including drug development and synthesis of more complex molecules. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.
Formula:C16H15NO2
InChI:InChI=1S/C16H15NO2/c18-16(19-12-13-6-2-1-3-7-13)17-11-10-14-8-4-5-9-15(14)17/h1-9H,10-12H2
InChI key:InChIKey=NWNPYJBRVCYRMG-UHFFFAOYSA-N
SMILES:C(OCC1=CC=CC=C1)(=O)N2C=3C(CC2)=CC=CC3
Synonyms:- Phenylmethyl 2,3-dihydro-1H-indole-1-carboxylate
- N-Benzyloxycarbonylindoline
- 1H-Indole-1-carboxylic acid, 2,3-dihydro-, phenylmethyl ester
- 2,3-Dihydro-indole-1-carboxylic acid benzyl ester
- 1-Benzyloxycarbonyl-2,3-dihydro-1H-indole
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