4-(tert-Butoxycarbonyl)-5,6-dihydro-4H-thieno[3,2-b]pyrrole-2-carboxylic acid

95%

  • Product Code: 87448
  CAS:    1250999-99-5
Molecular Weight: 269.32 g./mol Molecular Formula: C₁₂H₁₅NO₄S
EC Number: MDL Number: MFCD14581111
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, sealed, dry
Product Description: This compound is primarily utilized in the field of organic synthesis as a key intermediate in the development of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid functional group, makes it particularly valuable in peptide synthesis and the preparation of heterocyclic compounds. The Boc group is commonly used to protect amines during multi-step synthetic processes, ensuring selective reactions at other sites. Additionally, the thienopyrrole moiety in its structure is of interest in medicinal chemistry, where it can be incorporated into drug candidates targeting various biological pathways, such as enzyme inhibition or receptor modulation. Its carboxylic acid group also allows for further functionalization, enabling the creation of amides, esters, or other derivatives for diverse applications in pharmaceutical research and material science.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿17,550.00
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4-(tert-Butoxycarbonyl)-5,6-dihydro-4H-thieno[3,2-b]pyrrole-2-carboxylic acid
This compound is primarily utilized in the field of organic synthesis as a key intermediate in the development of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid functional group, makes it particularly valuable in peptide synthesis and the preparation of heterocyclic compounds. The Boc group is commonly used to protect amines during multi-step synthetic processes, ensuring selective reactions at other sites. Additionally, the thienopyrrole moiety in its structure is of interest in medicinal chemistry, where it can be incorporated into drug candidates targeting various biological pathways, such as enzyme inhibition or receptor modulation. Its carboxylic acid group also allows for further functionalization, enabling the creation of amides, esters, or other derivatives for diverse applications in pharmaceutical research and material science.
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