2-Methyl-3,5-bis(trifluoromethyl)aniline

97%

  • Product Code: 71998
  CAS:    243128-44-1
Molecular Weight: 243.15 g./mol Molecular Formula: C₉H₇F₆N
EC Number: MDL Number: MFCD00729099
Melting Point: Boiling Point: 193.1°C
Density: Storage Condition: 2-8°C
Product Description: Used primarily in the synthesis of pharmaceuticals, this compound serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its trifluoromethyl groups enhance the metabolic stability and bioavailability of the resulting drugs, making it valuable in medicinal chemistry. In agrochemicals, it is employed to develop herbicides and pesticides. The presence of trifluoromethyl groups contributes to the effectiveness and selectivity of these compounds, ensuring targeted action against pests and weeds while minimizing environmental impact. Additionally, it finds application in material science, particularly in the creation of specialty polymers and coatings. The unique electronic properties imparted by the trifluoromethyl groups improve the durability and performance of these materials in demanding environments. Its role in organic synthesis is also notable, where it acts as a building block for complex molecules in research and industrial processes, facilitating the development of novel compounds with specific functionalities.
Product Specification:
Test Specification
APPEARANCE Yellow to Brown solid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $191.91
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1.000 10-20 days $526.18
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2-Methyl-3,5-bis(trifluoromethyl)aniline
Used primarily in the synthesis of pharmaceuticals, this compound serves as a key intermediate in the production of various active pharmaceutical ingredients (APIs). Its trifluoromethyl groups enhance the metabolic stability and bioavailability of the resulting drugs, making it valuable in medicinal chemistry. In agrochemicals, it is employed to develop herbicides and pesticides. The presence of trifluoromethyl groups contributes to the effectiveness and selectivity of these compounds, ensuring targeted action against pests and weeds while minimizing environmental impact. Additionally, it finds application in material science, particularly in the creation of specialty polymers and coatings. The unique electronic properties imparted by the trifluoromethyl groups improve the durability and performance of these materials in demanding environments. Its role in organic synthesis is also notable, where it acts as a building block for complex molecules in research and industrial processes, facilitating the development of novel compounds with specific functionalities.
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