3-(Trifluoromethoxy)phenylboronic acid

98%

  • Product Code: 90023
  Alias:    3-(Trifluoromethoxy)phenylboronic acid
  CAS:    179113-90-7
Molecular Weight: 205.93 g./mol Molecular Formula: C₇H₆BF₃O₃
EC Number: MDL Number: MFCD01320697
Melting Point: 84-89 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the production of agrochemicals, contributing to the creation of herbicides and pesticides with enhanced efficacy. Additionally, it finds application in material science for the development of advanced polymers and coatings with improved chemical resistance and durability. Its trifluoromethoxy group enhances the stability and reactivity of the resulting compounds, making it valuable in various industrial and research applications.
Product Specification:
Test Specification
PURITYHPLC 98 100%
PURITYTITRATION BY NAOH 98 100%
APPEARANCE White to light brown powder or crystals
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿300.00
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-
5.000 10-20 days ฿980.00
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-
3-(Trifluoromethoxy)phenylboronic acid
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the production of agrochemicals, contributing to the creation of herbicides and pesticides with enhanced efficacy. Additionally, it finds application in material science for the development of advanced polymers and coatings with improved chemical resistance and durability. Its trifluoromethoxy group enhances the stability and reactivity of the resulting compounds, making it valuable in various industrial and research applications.
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