3-[[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-(4-methyl-cyclohexanecarbonyl)-amino]-5-iodo-thiophene-2-carboxylic acid methyl ester

95%

  • Product Code: 78656
  CAS:    1263101-57-0
Molecular Weight: 619.7 g./mol Molecular Formula: C₂₆H₄₂INO₄SSi
EC Number: MDL Number:
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Density: Storage Condition: 2-8°C, dry, airtight
Product Description: This compound is primarily utilized in organic synthesis and pharmaceutical research due to its complex structure, which makes it suitable for developing novel therapeutic agents. Its functional groups, including the tert-butyl-dimethyl-silanyloxy and iodo-thiophene moieties, enable it to act as an intermediate in the synthesis of biologically active molecules. It is particularly valuable in the development of targeted drugs, where its unique structure can be modified to enhance binding affinity and selectivity. Additionally, its ester group allows for further chemical modifications, making it a versatile building block in medicinal chemistry. Researchers often employ it in the study of enzyme inhibitors and receptor modulators, leveraging its potential to interact with specific biological targets.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days €1,086.52
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3-[[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-(4-methyl-cyclohexanecarbonyl)-amino]-5-iodo-thiophene-2-carboxylic acid methyl ester
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its complex structure, which makes it suitable for developing novel therapeutic agents. Its functional groups, including the tert-butyl-dimethyl-silanyloxy and iodo-thiophene moieties, enable it to act as an intermediate in the synthesis of biologically active molecules. It is particularly valuable in the development of targeted drugs, where its unique structure can be modified to enhance binding affinity and selectivity. Additionally, its ester group allows for further chemical modifications, making it a versatile building block in medicinal chemistry. Researchers often employ it in the study of enzyme inhibitors and receptor modulators, leveraging its potential to interact with specific biological targets.
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