Ethyl (1R,2R)-2-(tert-butoxycarbonylamino)cyclopentanecarboxylate
95%
- Product Code: 70790
CAS:
245115-20-2
Molecular Weight: | 257.33 g./mol | Molecular Formula: | C₁₃H₂₃NO₄ |
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EC Number: | MDL Number: | MFCD19689414 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various drugs, including antiviral and anticancer agents. Its structure, featuring a cyclopentane ring and protective groups, makes it valuable for constructing specific chiral centers and maintaining stereochemistry during multi-step synthetic processes. Additionally, it is employed in peptide synthesis, where the tert-butoxycarbonyl (Boc) group acts as a protective moiety for amino functionalities, ensuring selective reactions in the formation of peptide bonds. Its versatility and stability make it a crucial component in medicinal chemistry and organic synthesis.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿11,700.00 |
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0.250 | 10-20 days | ฿22,500.00 |
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1.000 | 10-20 days | ฿45,000.00 |
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Ethyl (1R,2R)-2-(tert-butoxycarbonylamino)cyclopentanecarboxylate
This compound is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various drugs, including antiviral and anticancer agents. Its structure, featuring a cyclopentane ring and protective groups, makes it valuable for constructing specific chiral centers and maintaining stereochemistry during multi-step synthetic processes. Additionally, it is employed in peptide synthesis, where the tert-butoxycarbonyl (Boc) group acts as a protective moiety for amino functionalities, ensuring selective reactions in the formation of peptide bonds. Its versatility and stability make it a crucial component in medicinal chemistry and organic synthesis.
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