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4815-29-6

Ethyl 2-amino-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate

Catalog#: AR003QSA  |   CAS#: 4815-29-6  |   MDL#: MFCD00102063  |   MF: C10H13NO2S  |   MW: 211.28072

Packsize Purity Price Availability Quantity
250mg 96% $4.00 Global Stock Buy Now Add To Cart
1g 96% $4.00 Global Stock Buy Now Add To Cart
5g 96% $12.00 Global Stock Buy Now Add To Cart
10g 96% $19.00 Global Stock Buy Now Add To Cart
100g 96% $159.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003QSA
Chemical Name Ethyl 2-amino-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate
CAS Number 4815-29-6
Molecular Formula C10H13NO2S
Molecular Weight 211.28072
MDL Number MFCD00102063
SMILES CCOC(=O)c1c(N)sc2c1CCC2
NSC Number 99004

Ethyl 2-amino-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate is a valuable compound widely used in chemical synthesis due to its versatile reactivity and unique structural properties. With its cyclic structure containing both amino and ester functional groups, this compound serves as a key building block in the synthesis of various heterocyclic compounds and pharmaceutical intermediates.In organic synthesis, Ethyl 2-amino-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate can participate in a range of reactions including acylation, alkylation, cyclization, and condensation reactions. Its presence of the amino group allows for facile derivatization, enabling the introduction of different substituents and the generation of diverse molecular scaffolds. Additionally, the conjugated system in the cyclopentathiophene ring offers opportunities for further functionalization and manipulation of its electronic properties.Overall, the application of Ethyl 2-amino-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate in chemical synthesis extends beyond its initial structure, allowing for the synthesis of intricate molecules with tailored properties for a variety of industrial and scientific purposes.
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