Copper(I) Trifluoromethanethiolate

≥90%

  • Product Code: 79649
  CAS:    3872-23-9
Molecular Weight: 164.61 g./mol Molecular Formula: CCuF₃S
EC Number: MDL Number: MFCD00059046
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: Copper(I) trifluoromethanethiolate is primarily used in organic synthesis as a reagent for introducing the trifluoromethylthio group (-SCF3) into various molecules. This group is highly valuable in medicinal chemistry and agrochemical research due to its strong electron-withdrawing properties and ability to enhance the metabolic stability and lipophilicity of compounds. It is particularly effective in cross-coupling reactions, enabling the synthesis of complex molecules with potential pharmaceutical applications. Additionally, it is employed in the preparation of advanced materials, where the trifluoromethylthio group can modify the electronic properties of polymers or small molecules for use in electronics or coatings. Its role in facilitating efficient and selective transformations makes it a key tool in modern synthetic chemistry.
Product Specification:
Test Specification
APPEARANCE White to Light yellow to Light orange powder to crystal
PURITY 89.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days $337.67
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1.000 10-20 days $1,077.82
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Copper(I) Trifluoromethanethiolate
Copper(I) trifluoromethanethiolate is primarily used in organic synthesis as a reagent for introducing the trifluoromethylthio group (-SCF3) into various molecules. This group is highly valuable in medicinal chemistry and agrochemical research due to its strong electron-withdrawing properties and ability to enhance the metabolic stability and lipophilicity of compounds. It is particularly effective in cross-coupling reactions, enabling the synthesis of complex molecules with potential pharmaceutical applications. Additionally, it is employed in the preparation of advanced materials, where the trifluoromethylthio group can modify the electronic properties of polymers or small molecules for use in electronics or coatings. Its role in facilitating efficient and selective transformations makes it a key tool in modern synthetic chemistry.
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