10592-27-5
Chemical Structure
2,3-Dihydro-7-azaindole
Synonym(s): 7-Azaindoline
- CAS. Nr.: 10592-27-5
- Formula:C7H8N2
- Molecular Weight:120.16
IUPAC Name: 2,3-dihydro-1H-pyrrolo[2,3-b]pyridine
InChIKey: ZFFYPGZDXUPKNK-UHFFFAOYSA-N
SMILES: C12=CC=CN=C1NCC2
Biological Activity: 2,3-Dihydro-7-azaindole (7-Azaindoline) is a cyclic secondary amine substrate with a fused aromatic ring, which serves as a substrate for hydrogenation reactions. 2,3-Dihydro-7-azaindole undergoes amidation with methyl pyrazine-2-carboxylate under the catalysis of lipase from Pseudomonas stutzeri. 2,3-Dihydro-7-azaindole is often used as an intermediate in organic synthesis, for example, in the preparation of indole compounds[1][2].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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2,3-Dihydro-7-azaindole | 99.96% | 2,3-Dihydro-7-azaindole (7-Azaindoline) is a cyclic secondary amine substrate with a fused aromatic ring, which serves as a substrate for hydrogenation reactions. 2,3-Dihydro-7-azaindole undergoes amidation with methyl pyrazine-2-carboxylate under the catalysis of lipase from Pseudomonas stutzeri. 2,3-Dihydro-7-azaindole is often used as an intermediate in organic synthesis, for example, in the preparation of indole compounds. | ||||||||||||||||||||
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References
- [1]. Kumar A, et al. Biocarbon Supported Nanoscale Ruthenium Oxide‑Based Catalyst for Clean Hydrogenation of Arenes and Heteroarenes. ACS Sustainable Chem. Eng., 2020, 8(41):15740‑15754.
- [2]. Paggiola G, et al. Application of bio‑based solvents for biocatalysed synthesis of amides with Pseudomonas stutzeri lipase (PSL). Pure and Applied Chemistry, 2019, 92:579‑586.
