2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azaheptadecan-17-oic acid

97%

  • Product Code: 40542
  CAS:    1347750-75-7
Molecular Weight: 321.37 g./mol Molecular Formula: C₁₄H₂₇NO₇
EC Number: MDL Number: MFCD24539476
Melting Point: Boiling Point: 471.1±40.0 °C(Predicted)
Density: 1.124±0.06 g/cm3(Predicted) Storage Condition: 2-8°C, dry, sealed
Product Description: This chemical is primarily used in the synthesis of complex organic compounds, particularly in the field of pharmaceutical research. It serves as a key intermediate in the production of certain drugs, especially those targeting specific enzymatic pathways or receptors. Its structure, featuring multiple oxygen and nitrogen atoms, makes it suitable for creating molecules with enhanced bioavailability and stability. Additionally, it is utilized in the development of biodegradable polymers and surfactants due to its amphiphilic properties. In material science, it contributes to the design of advanced coatings and adhesives with improved performance characteristics. Its versatility also extends to biochemical applications, where it is employed as a building block for peptide analogs and other bioactive molecules.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days €60.78
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1.000 10-20 days €158.61
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2,2-Dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azaheptadecan-17-oic acid
This chemical is primarily used in the synthesis of complex organic compounds, particularly in the field of pharmaceutical research. It serves as a key intermediate in the production of certain drugs, especially those targeting specific enzymatic pathways or receptors. Its structure, featuring multiple oxygen and nitrogen atoms, makes it suitable for creating molecules with enhanced bioavailability and stability. Additionally, it is utilized in the development of biodegradable polymers and surfactants due to its amphiphilic properties. In material science, it contributes to the design of advanced coatings and adhesives with improved performance characteristics. Its versatility also extends to biochemical applications, where it is employed as a building block for peptide analogs and other bioactive molecules.
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