3-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid
95%
- Product Code: 104513
CAS:
776330-74-6
Molecular Weight: | 257.33 g./mol | Molecular Formula: | C₁₃H₂₃NO₄ |
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EC Number: | MDL Number: | MFCD06410607 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps protect amino groups during chemical reactions. The cyclopentyl moiety contributes to the compound's ability to modulate the pharmacokinetic properties of drug candidates, enhancing their stability and bioavailability. It is often employed in the preparation of small-molecule inhibitors and therapeutic agents targeting specific enzymes or receptors. Additionally, its carboxylic acid functionality allows for further derivatization, enabling the creation of diverse chemical libraries for drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,759.00 |
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0.250 | 10-20 days | ฿10,152.00 |
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1.000 | 10-20 days | ฿20,151.00 |
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3-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in peptide synthesis, where it helps protect amino groups during chemical reactions. The cyclopentyl moiety contributes to the compound's ability to modulate the pharmacokinetic properties of drug candidates, enhancing their stability and bioavailability. It is often employed in the preparation of small-molecule inhibitors and therapeutic agents targeting specific enzymes or receptors. Additionally, its carboxylic acid functionality allows for further derivatization, enabling the creation of diverse chemical libraries for drug discovery.
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