CAS 5599-71-3
:3,6-dichloro-9H-carbazole
Description:
3,6-Dichloro-9H-carbazole is an organic compound characterized by its structure, which features a carbazole backbone with chlorine substituents at the 3 and 6 positions. This compound is typically a solid at room temperature and exhibits a crystalline form. It is known for its relatively high thermal stability and can be soluble in organic solvents such as chloroform and dichloromethane, but is generally insoluble in water. The presence of chlorine atoms enhances its electronic properties, making it of interest in various applications, including organic electronics and as a potential intermediate in the synthesis of dyes and pigments. Additionally, 3,6-dichloro-9H-carbazole may exhibit photoluminescent properties, which can be advantageous in optoelectronic devices. Safety considerations should be taken into account, as with many chlorinated compounds, due to potential toxicity and environmental impact. Proper handling and disposal methods are essential to mitigate any risks associated with its use.
Formula:C12H7Cl2N
InChI:InChI=1/C12H7Cl2N/c13-7-1-3-11-9(5-7)10-6-8(14)2-4-12(10)15-11/h1-6,15H
SMILES:c1cc2c(cc1Cl)c1cc(ccc1[nH]2)Cl
Synonyms:- 3,6-Dichlorocarbazole
- 9H-carbazole, 3,6-dichloro-
- Carbazole, 3,6-dichloro-
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Found 6 products.
3,6-Dichlorocarbazole
CAS:Formula:C12H7Cl2NPurity:>96.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:236.103,6-Dichloro-9H-carbazole
CAS:Formula:C12H7Cl2NPurity:96%Color and Shape:SolidMolecular weight:236.09673,6-dichloro-9H-carbazole
CAS:Purity:96.0%Color and Shape:Solid, White to slightly pale reddish yellow powderMolecular weight:236.100006103515623,6-Dichlorocarbazole
CAS:<p>3,6-Dichlorocarbazole is a potential mechanism that has been shown to be degradable in chlorine. The median concentration of 3,6-dichlorocarbazole in the dry weight of marine organisms is 0.0007% and it reacts at an average rate of 10%. 3,6-Dichlorocarbazole has been observed to have anthropogenic origins and can be found in low concentrations in the environment. There are four isomers that are produced by this reaction: 2,4-, 2,5-, 2,6-, and 3,4-dichlorocarbazole. <br>3,6-Dichlorocarbazole has been shown to cause functional changes in organisms due to its effects on gene transcription. This chemical has been shown to alter the transcriptomic profile of a number of gene families involved with cellular stress response pathways in both aquatic invertebrates and fish.</p>Formula:C12H7Cl2NPurity:Min. 96 Area-%Molecular weight:236.1 g/mol




