(1S,3S)-Methyl 3-aminocyclopentanecarboxylate hydrochloride

97%

  • Product Code: 113036
  CAS:    1085842-51-8
Molecular Weight: 179.65 g./mol Molecular Formula: C₇H₁₄ClNO₂
EC Number: MDL Number: MFCD23106008
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, dry and sealed
Product Description: This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring both amino and ester functional groups, makes it a versatile building block for the development of cyclopentane-based drugs. It is particularly valuable in the creation of antiviral and anticancer agents, where the cyclopentane ring contributes to the stability and specificity of the active pharmaceutical ingredients. Additionally, its chiral centers allow for the production of enantiomerically pure compounds, which is crucial for ensuring the efficacy and safety of therapeutic drugs. Researchers also employ this chemical in medicinal chemistry studies to explore novel drug candidates targeting specific biological pathways.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $441.64
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0.250 10-20 days $1,059.57
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(1S,3S)-Methyl 3-aminocyclopentanecarboxylate hydrochloride
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring both amino and ester functional groups, makes it a versatile building block for the development of cyclopentane-based drugs. It is particularly valuable in the creation of antiviral and anticancer agents, where the cyclopentane ring contributes to the stability and specificity of the active pharmaceutical ingredients. Additionally, its chiral centers allow for the production of enantiomerically pure compounds, which is crucial for ensuring the efficacy and safety of therapeutic drugs. Researchers also employ this chemical in medicinal chemistry studies to explore novel drug candidates targeting specific biological pathways.
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