CAS 203385-15-3

ethyl 2-[(chloroacetyl)amino]-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate

Description:

Ethyl 2-[(chloroacetyl)amino]-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate, with CAS number 203385-15-3, is a chemical compound characterized by its unique structure that includes a cyclopentathiophene core. This compound features a chloroacetylamino group, which contributes to its reactivity and potential biological activity. The presence of the ethyl ester group enhances its solubility in organic solvents, making it suitable for various applications in organic synthesis and medicinal chemistry. The thiophene ring system is known for its electronic properties, which can influence the compound's behavior in chemical reactions and interactions with biological targets. Additionally, the compound may exhibit specific pharmacological activities, although detailed studies would be necessary to elucidate its full biological profile. Overall, this compound represents a class of heterocyclic compounds that are of interest in drug development and materials science due to their diverse chemical properties and potential applications.

Formula: C₁₂H₁₄ClNO₃S

InChI: InChI=1/C12H14ClNO3S/c1-2-17-12(16)10-7-4-3-5-8(7)18-11(10)14-9(15)6-13/h2-6H2,1H3,(H,14,15)

SMILES: CCOC(=O)c1c2CCCc2sc1N=C(CCl)O

Synonyms:

• 2-(2-Chloro-Acetylamino)-5,6-Dihydro-4H-Cyclopenta[B]Thiophene-3-Carboxylic Acid Ethyl Ester
• 4H-Cyclopenta[b]thiophene-3-carboxylic acid, 2-[(2-chloroacetyl)amino]-5,6-dihydro-, ethyl ester
• Ethyl 2-[(chloroacetyl)amino]-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate

4H-Cyclopenta[b]thiophene-3-carboxylic acid, 2-[(2-chloroacetyl)amino]-5,6-dihydro-, ethyl ester

CAS: 203385-15-3

Formula: C₁₂H₁₄ClNO₃S

Purity: 97%

Molecular weight: 287.7625

Ref: IN-DA0028UJ

2-(2-Chloro-acetylamino)-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylic acid ethyl ester

CAS: 203385-15-3

Formula: C₁₂H₁₄ClNO₃S

Purity: 95.0%

Molecular weight: 287.76

Ref: 10-F344776