(1R,3S)-Cyclopentane-1,3-dicarboxylic acid

≥95%

  • Product Code: 123377
  CAS:    876-05-1
Molecular Weight: 158.15 g./mol Molecular Formula: C₇H₁₀O₄
EC Number: MDL Number: MFCD01311175
Melting Point: Boiling Point: 320.7°C at 760 mmHg
Density: Storage Condition: Room temperature, dry and sealed
Product Description: This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a chiral building block for the development of enantiomerically pure drugs, which are crucial for ensuring specific biological activity and reducing side effects. Its rigid cyclopentane structure and carboxylic acid functional groups make it a valuable intermediate in the production of bioactive compounds, such as antiviral and anti-inflammatory agents. Additionally, it is employed in research for designing peptide mimetics and other small molecules that target specific enzymes or receptors. Its stereochemistry also plays a key role in asymmetric synthesis, enabling the creation of highly selective and efficient chemical reactions.
Product Specification:
Test Specification
Appearance White To Yellow Powder Or Crystals
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿1,220.00
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-
1.000 10-20 days ฿2,330.00
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-
5.000 10-20 days ฿10,830.00
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-
(1R,3S)-Cyclopentane-1,3-dicarboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a chiral building block for the development of enantiomerically pure drugs, which are crucial for ensuring specific biological activity and reducing side effects. Its rigid cyclopentane structure and carboxylic acid functional groups make it a valuable intermediate in the production of bioactive compounds, such as antiviral and anti-inflammatory agents. Additionally, it is employed in research for designing peptide mimetics and other small molecules that target specific enzymes or receptors. Its stereochemistry also plays a key role in asymmetric synthesis, enabling the creation of highly selective and efficient chemical reactions.
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