(1S,4R)-4-Aminocyclopent-2-enecarboxylic acid
≥95%
- Product Code: 36270
CAS:
134234-04-1
Molecular Weight: | 127.14 g./mol | Molecular Formula: | C₆H₉NO₂ |
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EC Number: | MDL Number: | MFCD00211286 | |
Melting Point: | Boiling Point: | 266.6±40.0°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
(1S,4R)-4-Aminocyclopent-2-enecarboxylic acid is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate or building block in the synthesis of various pharmaceutical compounds. Its unique structure, featuring both an amino group and a carboxylic acid on a cyclopentene ring, makes it valuable for designing molecules with specific biological activities.
One of its notable applications is in the development of enzyme inhibitors, particularly those targeting enzymes involved in metabolic pathways or disease mechanisms. The compound's rigid cyclic structure and functional groups allow it to mimic natural substrates, making it useful in creating potent and selective inhibitors. Additionally, it has been explored in the synthesis of prodrugs and bioactive molecules for treating neurological disorders, inflammation, and infections. Its versatility in chemical modifications further enhances its role in optimizing drug candidates for improved efficacy and safety.
Product Specification:
Test | Specification |
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APPEARANCE | Off-white to light brown Solid |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿580.00 |
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0.250 | 10-20 days | ฿870.00 |
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1.000 | 10-20 days | ฿2,180.00 |
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5.000 | 10-20 days | ฿8,980.00 |
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(1S,4R)-4-Aminocyclopent-2-enecarboxylic acid
(1S,4R)-4-Aminocyclopent-2-enecarboxylic acid is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate or building block in the synthesis of various pharmaceutical compounds. Its unique structure, featuring both an amino group and a carboxylic acid on a cyclopentene ring, makes it valuable for designing molecules with specific biological activities.
One of its notable applications is in the development of enzyme inhibitors, particularly those targeting enzymes involved in metabolic pathways or disease mechanisms. The compound's rigid cyclic structure and functional groups allow it to mimic natural substrates, making it useful in creating potent and selective inhibitors. Additionally, it has been explored in the synthesis of prodrugs and bioactive molecules for treating neurological disorders, inflammation, and infections. Its versatility in chemical modifications further enhances its role in optimizing drug candidates for improved efficacy and safety.
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