(1S,2R)-2-(Boc-amino)cyclopentanecarboxylic Acid
≥97%
- Product Code: 76129
CAS:
137170-89-9
Molecular Weight: | 229.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
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EC Number: | MDL Number: | MFCD09750528 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
(1S,2R)-2-(Boc-amino)cyclopentanecarboxylic Acid is widely used in the synthesis of peptides and peptidomimetics. It serves as a key intermediate in the preparation of complex molecules, particularly in the development of pharmaceuticals. The Boc (tert-butoxycarbonyl) protecting group ensures selective reactivity during peptide coupling reactions, making it valuable in solid-phase peptide synthesis. This compound is also employed in the creation of cyclic peptide structures, which are important in drug discovery due to their enhanced stability and bioavailability. Additionally, it is utilized in the study of enzyme inhibitors and receptor ligands, contributing to the development of targeted therapies for various diseases. Its chiral structure makes it particularly useful in asymmetric synthesis, enabling the production of enantiomerically pure compounds.
Product Specification:
Test | Specification |
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APPEARANCE | White powder |
PURITY | 97-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿2,200.00 |
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1.000 | 10-20 days | ฿6,800.00 |
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(1S,2R)-2-(Boc-amino)cyclopentanecarboxylic Acid
(1S,2R)-2-(Boc-amino)cyclopentanecarboxylic Acid is widely used in the synthesis of peptides and peptidomimetics. It serves as a key intermediate in the preparation of complex molecules, particularly in the development of pharmaceuticals. The Boc (tert-butoxycarbonyl) protecting group ensures selective reactivity during peptide coupling reactions, making it valuable in solid-phase peptide synthesis. This compound is also employed in the creation of cyclic peptide structures, which are important in drug discovery due to their enhanced stability and bioavailability. Additionally, it is utilized in the study of enzyme inhibitors and receptor ligands, contributing to the development of targeted therapies for various diseases. Its chiral structure makes it particularly useful in asymmetric synthesis, enabling the production of enantiomerically pure compounds.
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