4-Isopropoxy-3-(trifluoromethyl)benzoic acid

97%

  • Product Code: 118886
  CAS:    213598-16-4
Molecular Weight: 248.20 g./mol Molecular Formula: C₁₁H₁₁F₃O₃
EC Number: MDL Number: MFCD12913405
Melting Point: Boiling Point: 312.4°C at 760 mmHg
Density: 1.287g/cm3 Storage Condition: Room temperature, dry and sealed
Product Description: This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a trifluoromethyl group and an isopropoxy moiety, makes it valuable for designing molecules with enhanced biological activity and stability. It is often employed in the development of active pharmaceutical ingredients (APIs) where the trifluoromethyl group can improve metabolic resistance and binding affinity to target proteins. Additionally, it serves as a key building block in the synthesis of herbicides and pesticides, contributing to the creation of more effective and selective crop protection agents. Its versatility in chemical reactions, such as coupling and functional group transformations, further underscores its importance in advanced chemical research and industrial applications.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days £18.93
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0.250 10-20 days £33.38
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1.000 10-20 days £85.49
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5.000 10-20 days £382.88
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4-Isopropoxy-3-(trifluoromethyl)benzoic acid
This compound is primarily utilized in the field of organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring a trifluoromethyl group and an isopropoxy moiety, makes it valuable for designing molecules with enhanced biological activity and stability. It is often employed in the development of active pharmaceutical ingredients (APIs) where the trifluoromethyl group can improve metabolic resistance and binding affinity to target proteins. Additionally, it serves as a key building block in the synthesis of herbicides and pesticides, contributing to the creation of more effective and selective crop protection agents. Its versatility in chemical reactions, such as coupling and functional group transformations, further underscores its importance in advanced chemical research and industrial applications.
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