(R)-2-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid

95%

  • Product Code: 37454
  CAS:    219819-74-6
Molecular Weight: 257.3300 g./mol Molecular Formula: C₁₃H₂₃NO₄
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Density: Storage Condition: room temperature
Product Description: (R)-2-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid is primarily used in the synthesis of peptides and other biologically active molecules. It serves as a key intermediate in the production of pharmaceuticals, particularly in the development of drugs targeting specific enzymes or receptors. Its structure, featuring a cyclopentyl group and a Boc-protected amino group, makes it valuable for constructing complex molecules with precise stereochemistry. This compound is often employed in medicinal chemistry research to create analogs and derivatives for testing therapeutic efficacy. Additionally, it is utilized in the preparation of peptidomimetics, which are compounds designed to mimic the structure and function of peptides, enhancing drug stability and bioavailability. Its role in organic synthesis extends to the creation of chiral building blocks, which are essential for producing enantiomerically pure substances in drug development.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿1,755.00
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(R)-2-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid
(R)-2-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid is primarily used in the synthesis of peptides and other biologically active molecules. It serves as a key intermediate in the production of pharmaceuticals, particularly in the development of drugs targeting specific enzymes or receptors. Its structure, featuring a cyclopentyl group and a Boc-protected amino group, makes it valuable for constructing complex molecules with precise stereochemistry. This compound is often employed in medicinal chemistry research to create analogs and derivatives for testing therapeutic efficacy. Additionally, it is utilized in the preparation of peptidomimetics, which are compounds designed to mimic the structure and function of peptides, enhancing drug stability and bioavailability. Its role in organic synthesis extends to the creation of chiral building blocks, which are essential for producing enantiomerically pure substances in drug development.
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