(S)-(-)-6-HYDROXY-2,5,7,8-TETRAMETHYLCHROMAN-2-CARBOXYLIC ACID
98%
- Product Code: 71074
CAS:
53174-06-4
Molecular Weight: | 250.29 g./mol | Molecular Formula: | C₁₄H₁₈O₄ |
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EC Number: | MDL Number: | MFCD00180756 | |
Melting Point: | 160 °C (dec.)(lit.) | Boiling Point: | 450.3 °C at 760 mmHg |
Density: | 1.219 g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of antioxidants and bioactive molecules. Its chiral structure makes it valuable in the development of enantioselective drugs, particularly those targeting oxidative stress-related conditions. Additionally, it is employed in the synthesis of advanced materials with potential applications in biomedicine, such as drug delivery systems or coatings with antioxidant properties. Its role in research also extends to studying free radical scavenging mechanisms, contributing to the development of therapies for diseases linked to oxidative damage.
Product Specification:
Test | Specification |
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APPEARANCE | White to Off-white to Pale beige to Light grey to Brown Powder and/or Chunks |
PURITY | 97.5-100.0 |
OPTICAL ROTATIONC1.2 EtOH | -68.0 -62.0 |
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 | ฿2,340.00 |
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0.250 | 10-20 days | ฿8,350.00 |
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(S)-(-)-6-HYDROXY-2,5,7,8-TETRAMETHYLCHROMAN-2-CARBOXYLIC ACID
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of antioxidants and bioactive molecules. Its chiral structure makes it valuable in the development of enantioselective drugs, particularly those targeting oxidative stress-related conditions. Additionally, it is employed in the synthesis of advanced materials with potential applications in biomedicine, such as drug delivery systems or coatings with antioxidant properties. Its role in research also extends to studying free radical scavenging mechanisms, contributing to the development of therapies for diseases linked to oxidative damage.
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