(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
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
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
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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