1-Trifluoromethyl-3,3-dimethyl-1,2-benziodoxole

97%

  • Product Code: 79319
  Alias:    Togni reagent
  CAS:    887144-97-0
Molecular Weight: 330.09 g./mol Molecular Formula: C₁₀H₁₀F₃IO
EC Number: MDL Number: MFCD10567056
Melting Point: Boiling Point:
Density: Storage Condition: 2~8℃
Product Description: This compound is primarily utilized in organic synthesis as a versatile trifluoromethylating agent. It enables the introduction of the trifluoromethyl group into various organic molecules, which is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances the metabolic stability, bioavailability, and lipophilicity of compounds, making it a key functional group in drug design. Additionally, it is employed in the synthesis of complex molecules, including natural products and fine chemicals, due to its efficiency and selectivity in reactions. Its use is especially prominent in the preparation of fluorine-containing compounds, which are increasingly important in modern chemistry.
Product Specification:
Test Specification
Purity 96.5 100%
Appearance White to Tan Solid, Powder, Crystals, Crystalline Powder and/or Chunks
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days Ft10,989.59
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1.000 10-20 days Ft34,046.18
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5.000 10-20 days Ft118,299.71
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1-Trifluoromethyl-3,3-dimethyl-1,2-benziodoxole
This compound is primarily utilized in organic synthesis as a versatile trifluoromethylating agent. It enables the introduction of the trifluoromethyl group into various organic molecules, which is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances the metabolic stability, bioavailability, and lipophilicity of compounds, making it a key functional group in drug design. Additionally, it is employed in the synthesis of complex molecules, including natural products and fine chemicals, due to its efficiency and selectivity in reactions. Its use is especially prominent in the preparation of fluorine-containing compounds, which are increasingly important in modern chemistry.
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