(1S,3aR,6aS)-2-(tert-Butoxycarbonyl)octahydrocyclopenta[c]pyrrole-1-carboxylic acid
95%
- Product Code: 96538
CAS:
597569-42-1
Molecular Weight: | 255.31 g./mol | Molecular Formula: | C₁₃H₂₁NO₄ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 386.0±25.0 °C(Predicted) | |
Density: | 1.196 g/cm3 | Storage Condition: | 2-8℃, dry |
Product Description:
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps protect amine groups during complex reactions. The compound is also utilized in the development of small molecule drugs, particularly those targeting neurological and cardiovascular disorders. Its stereochemistry and functional groups allow for precise modifications, enabling the creation of molecules with specific biological activities. Additionally, it plays a role in medicinal chemistry research for designing and optimizing drug candidates with improved efficacy and safety profiles.
Product Specification:
Test | Specification |
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APPEARANCE | White Solid |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿45,260.00 |
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(1S,3aR,6aS)-2-(tert-Butoxycarbonyl)octahydrocyclopenta[c]pyrrole-1-carboxylic acid
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps protect amine groups during complex reactions. The compound is also utilized in the development of small molecule drugs, particularly those targeting neurological and cardiovascular disorders. Its stereochemistry and functional groups allow for precise modifications, enabling the creation of molecules with specific biological activities. Additionally, it plays a role in medicinal chemistry research for designing and optimizing drug candidates with improved efficacy and safety profiles.
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