Ethyl (2-chlorophenyl)(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetate sulfate (1:1)(CAS: 1357474-92-0)

Ethyl (2-chlorophenyl)(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetate sulfate (1:1) is a crystalline compound with a molecular weight of approximately 518.72 g/mol. It has moderate solubility in organic solvents like ethanol and poor solubility in water. The compound is reactive towards nucleophiles and can undergo substitution reactions. It also shows electrophilic aromatic substitution properties.

Ethyl (2-chlorophenyl)(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetate sulfate (1:1) is synthesized through a multi-step process involving the coupling of a chlorophenyl moiety with a thienopyridine derivative. The reaction typically requires a base and a catalyst, such as a phase-transfer catalyst, to increase the yield and selectivity. The product is then derivatized with an acetic acid derivative and finally converted to the sulfate salt.

Ethyl (2-chlorophenyl)(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetate sulfate (1:1) is used in the pharmaceutical industry for the development of novel drugs. It may also find applications in the polymer industry for specialized polymer synthesis and modification. Additionally, it could be used in the semiconductor industry for specific chemical processes and in sensor technology for its unique chemical reactivity.

Handling Ethyl (2-chlorophenyl)(6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetate sulfate (1:1) requires appropriate personal protective equipment (PPE) such as gloves, safety goggles, and a lab coat. It should be handled in a well-ventilated area, such as a fume hood, to minimize inhalation risks. Spills should be cleaned up immediately using appropriate absorbent materials, and the area should be flushed with water. Always refer to the Safety Data Sheet (SDS) for detailed handling and disposal information.