(1S,4R)-Methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate
99%
- Product Code: 36272
CAS:
419563-22-7
| Molecular Weight: | 291.26 g./mol | Molecular Formula: | C₁₁H₁₇NO₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18252294 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
(1S,4R)-Methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic molecules. Its unique stereochemistry and functional groups make it valuable for constructing chiral compounds, particularly in the development of antiviral and anticancer drugs. The compound's cyclopentene ring and carboxylate group allow for versatile chemical modifications, enabling the creation of targeted therapeutic agents. Additionally, it is employed in research settings to study enzyme inhibition and receptor binding, contributing to the discovery of new drug candidates. Its role in asymmetric synthesis also highlights its importance in producing enantiomerically pure substances, which are critical for effective and safe medications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Pale Yellow Powder |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | $99.45 |
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| 0.250 | 10-20 days | $331.49 |
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| 1.000 | 10-20 days | $903.57 |
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| 10.000 | 10-20 days | $3,013.06 |
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(1S,4R)-Methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate
(1S,4R)-Methyl 4-aminocyclopent-2-enecarboxylate (2R,3R)-2,3-dihydroxysuccinate is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of complex organic molecules. Its unique stereochemistry and functional groups make it valuable for constructing chiral compounds, particularly in the development of antiviral and anticancer drugs. The compound's cyclopentene ring and carboxylate group allow for versatile chemical modifications, enabling the creation of targeted therapeutic agents. Additionally, it is employed in research settings to study enzyme inhibition and receptor binding, contributing to the discovery of new drug candidates. Its role in asymmetric synthesis also highlights its importance in producing enantiomerically pure substances, which are critical for effective and safe medications.
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