3-Chloro-2,5-dihydro-1H-1λ^6-thiophene-1,1-dione, with the CAS number 7311-87-7, is a heterocyclic compound featuring a thiophene ring that is substituted with a chlorine atom and two carbonyl groups. This compound exhibits characteristics typical of thiophene derivatives, including aromaticity and potential reactivity due to the presence of the electrophilic carbonyl groups. The chlorine substituent can influence the compound's reactivity and solubility, making it more polar compared to its non-chlorinated counterparts. The presence of the carbonyl groups suggests that it may participate in various chemical reactions, such as nucleophilic addition or condensation reactions. Additionally, the compound may exhibit biological activity, which is common among thiophene derivatives, making it of interest in pharmaceutical and agrochemical research. Its physical properties, such as melting point and solubility, would depend on the specific conditions and solvent used. Overall, 3-chloro-2,5-dihydro-1H-1λ^6-thiophene-1,1-dione is a versatile compound with potential applications in various fields of chemistry.

3-chloro-2,5-dihydro-1H-1lambda~6~-thiophene-1,1-dione

7311-87-7: 3-Chloro-2,5-dihydro-1H-1λ^6-thiophene-1,1-dione, with the CAS number 7311-87-7, is a heterocyclic compound featuring a thiophene ring that is substituted with a chlorine atom and two carbonyl groups. This compound exhibits characteristics typical of thiophene derivatives, including aromaticity and potential reactivity due to the presence of the electrophilic carbonyl groups. The chlorine substituent can influence the compound's reactivity and solubility, making it more polar compared to its non-chlorinated counterparts. The presence of the carbonyl groups suggests that it may participate in various chemical reactions, such as nucleophilic addition or condensation reactions. Additionally, the compound may exhibit biological activity, which is common among thiophene derivatives, making it of interest in pharmaceutical and agrochemical research. Its physical properties, such as melting point and solubility, would depend on the specific conditions and solvent used. Overall, 3-chloro-2,5-dihydro-1H-1λ^6-thiophene-1,1-dione is a versatile compound with potential applications in various fields of chemistry.

CAS 7311-87-7

3-chloro-2,5-dihydro-1H-1lambda~6~-thiophene-1,1-dione

3-Chloro-3-thiolene 1,1-dioxide

Ref: 54-OR0299