CAS 4290-90-8
:1-pentyl-1H-indole-2,3-dione
Description:
1-Pentyl-1H-indole-2,3-dione, with the CAS number 4290-90-8, is a synthetic compound belonging to the indole family, characterized by its indole core structure modified with a pentyl group and two carbonyl groups at the 2 and 3 positions. This compound exhibits properties typical of indole derivatives, including potential biological activity and interactions with various receptors. It is often studied for its pharmacological effects, particularly in the context of cannabinoid research, due to its structural similarities to naturally occurring cannabinoids. The presence of the pentyl group enhances its lipophilicity, which may influence its solubility and bioavailability. As a diketone, it may also participate in various chemical reactions, including nucleophilic additions and condensation reactions. Safety and handling precautions should be observed, as with many organic compounds, due to potential toxicity or reactivity. Overall, 1-pentyl-1H-indole-2,3-dione is of interest in both synthetic organic chemistry and medicinal chemistry research.
Formula:C13H15NO2
InChI:InChI=1/C13H15NO2/c1-2-3-6-9-14-11-8-5-4-7-10(11)12(15)13(14)16/h4-5,7-8H,2-3,6,9H2,1H3
SMILES:CCCCCN1c2ccccc2C(=O)C1=O
Synonyms:- 1H-indole-2,3-dione, 1-pentyl-
- 1-PENTYL-1H-INDOLE-2,3-DIONE
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Found 3 products.
1-Pentyl-1H-indole-2,3-dione
CAS:<p>1-Pentyl-1H-indole-2,3-dione is a synthetic cannabinoid that is used as a recreational drug. It has been shown to be thermally labile and can decompose at high temperatures. 1-Pentyl-1H-indole-2,3-dione is an acidic compound with a melting point of 79°C. The compound is also oxidant and therefore can react with other compounds to create new substances. This reaction can be accelerated by light or heat, which may result in the formation of hazardous products such as naphthalene.</p>Formula:C13H15NO2Purity:Min. 95%Molecular weight:217.26 g/mol
