Potassium trifluoro(3-((3-nitrophenyl)amino)-3-oxopropyl)borate

95%

  • Product Code: 91072
  CAS:    1705578-38-6
Molecular Weight: 300.0838696 g./mol Molecular Formula: C₉H₉BF₃KN₂O₃
EC Number: MDL Number: MFCD28805727
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: This chemical is primarily utilized in organic synthesis as a reagent for the introduction of trifluoromethyl groups into various organic compounds. Its unique structure allows it to act as a source of nucleophilic trifluoromethyl species, which is particularly valuable in the synthesis of pharmaceuticals and agrochemicals where the trifluoromethyl group can enhance the biological activity and metabolic stability of the compounds. Additionally, it is employed in the development of advanced materials, where the incorporation of fluorine atoms can significantly alter the physical and chemical properties, such as thermal stability and resistance to degradation. Its application in catalytic processes also highlights its role in facilitating more efficient and selective chemical transformations.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $1,034.66
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0.250 10-20 days $1,968.86
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1.000 10-20 days $5,413.36
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Potassium trifluoro(3-((3-nitrophenyl)amino)-3-oxopropyl)borate
This chemical is primarily utilized in organic synthesis as a reagent for the introduction of trifluoromethyl groups into various organic compounds. Its unique structure allows it to act as a source of nucleophilic trifluoromethyl species, which is particularly valuable in the synthesis of pharmaceuticals and agrochemicals where the trifluoromethyl group can enhance the biological activity and metabolic stability of the compounds. Additionally, it is employed in the development of advanced materials, where the incorporation of fluorine atoms can significantly alter the physical and chemical properties, such as thermal stability and resistance to degradation. Its application in catalytic processes also highlights its role in facilitating more efficient and selective chemical transformations.
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