CAS 15937-07-2
:2,3-Dihydro-5,6-dimethoxy-1H-indole
Description:
2,3-Dihydro-5,6-dimethoxy-1H-indole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features two methoxy groups (-OCH3) at the 5 and 6 positions of the indole ring, contributing to its chemical reactivity and solubility properties. The presence of the dihydro group indicates that it has a saturated bond in the indole framework, which can influence its stability and reactivity. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and pharmacology. The methoxy substituents can enhance lipophilicity, potentially affecting the compound's interaction with biological membranes. Additionally, the compound may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-donating nature of the methoxy groups. Overall, 2,3-Dihydro-5,6-dimethoxy-1H-indole is a versatile compound with potential applications in research and development within the fields of organic and medicinal chemistry.
Formula:C10H13NO2
InChI:InChI=1S/C10H13NO2/c1-12-9-5-7-3-4-11-8(7)6-10(9)13-2/h5-6,11H,3-4H2,1-2H3
InChI key:InChIKey=DPRMKYPHVPDUIH-UHFFFAOYSA-N
SMILES:O(C)C=1C=C2C(=CC1OC)NCC2
Synonyms:- 1H-indole, 2,3-dihydro-5,6-dimethoxy-
- 2,3-Dihydro-5,6-dimethoxy-1H-indole
- 5,6-Dimethoxyindoline
- Indoline, 5,6-dimethoxy-
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