CAS 88368-11-0
:6-chloro-1,2,3,9-tetrahydro-4H-carbazol-4-one
Description:
6-Chloro-1,2,3,9-tetrahydro-4H-carbazol-4-one is a chemical compound characterized by its unique bicyclic structure, which includes a carbazole moiety. This compound features a chloro substituent at the 6-position and a carbonyl group at the 4-position, contributing to its reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the chloro group can influence its electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions. The compound may also possess pharmacological properties, as many carbazole derivatives are known for their biological activities, including anti-inflammatory and anticancer effects. Its molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Safety and handling precautions should be observed, as with any chemical substance, due to potential toxicity or reactivity. Further studies would be necessary to fully elucidate its properties and applications in various fields.
Formula:C12H10ClNO
InChI:InChI=1/C12H10ClNO/c13-7-4-5-9-8(6-7)12-10(14-9)2-1-3-11(12)15/h4-6,14H,1-3H2
SMILES:C1Cc2c(c3cc(ccc3[nH]2)Cl)C(=O)C1
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-4-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H10ClNOPurity:Min. 95%Molecular weight:219.66 g/mol
