CAS 6960-42-5
:7-Nitroindole
Description:
7-Nitroindole is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring, with a nitro group (-NO2) positioned at the 7th carbon of the indole framework. This compound is typically a yellow crystalline solid and is known for its role in various chemical and biological applications, including as a building block in organic synthesis and as a potential fluorescent probe. 7-Nitroindole exhibits moderate solubility in organic solvents, and its reactivity is influenced by the presence of the nitro group, which can participate in electrophilic substitution reactions. Additionally, it has been studied for its potential pharmacological properties, including effects on neurotransmitter systems. The compound's molecular formula reflects its composition, and its physical properties, such as melting point and boiling point, can vary based on purity and environmental conditions. Overall, 7-Nitroindole is a significant compound in both synthetic chemistry and biological research.
Formula:C8H6N2O2
InChI:InChI=1S/C8H6N2O2/c11-10(12)7-3-1-2-6-4-5-9-8(6)7/h1-5,9H
InChI key:InChIKey=LZJGQIVWUKFTRD-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C2C(C=CN2)=CC=C1
Synonyms:- 1H-Indole, 7-nitro-
- 7-nitro-1H-indole
- Indole, 7-nitro-
- NSC 69874
- 7-Nitroindole
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Found 6 products.
7-Nitro-1H-indole
CAS:7-Nitro-1H-indoleFormula:C8H6N2O2Purity:≥95%Color and Shape: faint orange to yellow crystalline solidMolecular weight:162.15g/mol7-Nitroindole
CAS:Formula:C8H6N2O2Purity:>98.0%(GC)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:162.157-Nitroindole
CAS:Formula:C8H6N2O2Purity:97%Color and Shape:Solid, Crystalline Powder or Lumps or PowderMolecular weight:162.1487-Nitroindole
CAS:<p>7-Nitroindole is a hybridization analog of the base cytosine that has been used in biological studies. It has been shown to be active against microglia cells, which are involved in the inflammatory response. 7-Nitroindole's mechanism of action is not well understood; it may react with hydrochloric acid in the stomach to form nitrosamines and chloride ions, or it may react with hydrogen chloride to produce an ethyl ester. It also reacts with ethyl esters in the presence of light to form a photochemical reaction that generates fluorescence. The mechanism is not yet fully understood.</p>Formula:C8H6N2O2Color and Shape:PowderMolecular weight:162.15 g/mol





