CAS 82436-20-2
:2-(3-Bromophenyl)-1,3-dithiolane
Description:
2-(3-Bromophenyl)-1,3-dithiolane is an organic compound characterized by its unique structure, which includes a dithiolane ring and a bromophenyl substituent. The presence of the dithiolane moiety contributes to its potential reactivity, particularly in nucleophilic substitution reactions due to the electron-withdrawing nature of the bromine atom on the phenyl ring. This compound typically exhibits a moderate level of solubility in organic solvents, reflecting its non-polar characteristics. The bromine substituent can also influence the compound's physical properties, such as melting and boiling points, as well as its spectral characteristics in techniques like NMR and IR spectroscopy. Additionally, the compound may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Safety considerations should be taken into account due to the presence of bromine, which can pose health risks. Overall, 2-(3-Bromophenyl)-1,3-dithiolane is a versatile compound with potential applications in various fields, including organic synthesis and pharmaceuticals.
Formula:C9H9BrS2
InChI:InChI=1S/C9H9BrS2/c10-8-3-1-2-7(6-8)9-11-4-5-12-9/h1-3,6,9H,4-5H2
InChI key:InChIKey=JHRNZQWXJTUNHH-UHFFFAOYSA-N
SMILES:BrC=1C=C(C=CC1)C2SCCS2
Synonyms:- 2-(3-Bromophenyl)-1,3-dithiolane
- 1,3-Dithiolane, 2-(3-bromophenyl)-
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