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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > Ethyl 2-amino-4H,5H,7H-thieno[2,3-c]pyran-3-carboxylate

AE10912

117642-16-7 | Ethyl 2-amino-4H,5H,7H-thieno[2,3-c]pyran-3-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $10.00 $7.00 -   +
250mg 98% in stock $18.00 $13.00 -   +
1g 98% in stock $60.00 $42.00 -   +
5g 98% in stock $221.00 $155.00 -   +
25g 98% in stock $1,008.00 $706.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE10912
Chemical Name: Ethyl 2-amino-4H,5H,7H-thieno[2,3-c]pyran-3-carboxylate
CAS Number: 117642-16-7
Molecular Formula: C10H13NO3S
Molecular Weight: 227.2801
MDL Number: MFCD05664038
SMILES: CCOC(=O)c1c(N)sc2c1CCOC2

 

Computed Properties
Complexity: 249  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 1.7  

 

 

Upstream Synthesis Route
  • Ethyl 2-amino-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate is a powerful intermediate in chemical synthesis due to its versatile reactivity and unique structural features. This compound serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its functional groups and heterocyclic backbone make it a valuable starting material for the synthesis of complex molecules through various chemical transformations.In chemical synthesis, Ethyl 2-amino-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate can undergo a range of reactions such as condensations, cyclizations, and functional group manipulations to yield diverse organic compounds with desired properties. Its presence in a synthetic pathway can enable the creation of novel structures with specific biological activities or material properties. Additionally, this compound's structural motifs can facilitate the introduction of chirality or other important structural elements into target molecules, making it a strategic choice for designing and accessing new chemical entities.
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