CAS 16990-73-1
:1H-Indol-2-ol
Description:
1H-Indol-2-ol, also known as indole-2-ol, is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a hydroxyl (-OH) group attached to the second carbon of the indole ring, contributing to its classification as an indole derivative. It is typically a white to pale yellow solid with moderate solubility in water and higher solubility in organic solvents. The presence of the hydroxyl group imparts some polar characteristics, influencing its reactivity and interactions with other molecules. 1H-Indol-2-ol is of interest in various fields, including medicinal chemistry, due to its potential biological activities, such as antimicrobial and antioxidant properties. Additionally, it can serve as a building block in the synthesis of more complex organic compounds. Its chemical behavior is influenced by the indole framework, which is known for its aromaticity and ability to participate in various chemical reactions, including electrophilic substitutions and hydrogen bonding.
Formula:C8H7NO
InChI:InChI=1S/C8H7NO/c10-8-5-6-3-1-2-4-7(6)9-8/h1-5,9-10H
InChI key:InChIKey=JHFAEUICJHBVHB-UHFFFAOYSA-N
SMILES:OC1=CC=2C(N1)=CC=CC2
Synonyms:- 2-Hydroxyindole
- Indol-2-ol
- 1H-Indol-2-ol
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Found 3 products.
2-Hydroxyindole
CAS:<p>2-Hydroxyindole (2HI) is a potent antitumor agent that has been shown to inhibit the growth of prostate cancer cells. It binds to response elements and inhibits the production of growth factors, which are responsible for cell proliferation. 2HI also inhibits cancer cell proliferation by binding to the hydroxyl group on the aromatic ring and preventing DNA synthesis. The drug has been shown to be active against both basic fibroblast and activated T lymphocytes in vitro. 2-Hydroxyindole is an asymmetric synthesis with an activity index of 1.0, meaning it is equally potent in either direction of synthesis.</p>Formula:C8H7NOPurity:Min. 95%Color and Shape:PowderMolecular weight:133.15 g/mol
