2-Amino-3-cyclopropylpropanoic acid
98%
- Product Code: 76225
CAS:
15785-52-1
Molecular Weight: | 129.15 g./mol | Molecular Formula: | C₆H₁₁NO₂ |
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EC Number: | MDL Number: | MFCD02666085 | |
Melting Point: | Boiling Point: | 258°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, inflatable, dark |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological and cardiovascular disorders. Its cyclopropyl group enhances the stability and bioavailability of the resulting drugs, making it valuable for creating compounds with improved pharmacokinetic properties. Additionally, it is employed in the design of peptide-based therapeutics, where its unique structure contributes to the modulation of peptide conformation and activity. Researchers also explore its potential in developing enzyme inhibitors and receptor modulators due to its ability to mimic natural amino acids while introducing structural diversity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,503.00 |
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0.250 | 10-20 days | ฿2,160.00 |
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1.000 | 10-20 days | ฿5,508.00 |
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2-Amino-3-cyclopropylpropanoic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological and cardiovascular disorders. Its cyclopropyl group enhances the stability and bioavailability of the resulting drugs, making it valuable for creating compounds with improved pharmacokinetic properties. Additionally, it is employed in the design of peptide-based therapeutics, where its unique structure contributes to the modulation of peptide conformation and activity. Researchers also explore its potential in developing enzyme inhibitors and receptor modulators due to its ability to mimic natural amino acids while introducing structural diversity.
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