"fluorinated silane"
- 4 Items Found-
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TRICHLORO[3-(PENTAFLUOROPHENYL)PROPYL]SILANE (CAS NO. 78900-02-4)
1. High-performance Fluorosilicone Polymer Synthetic Monomer This product is a high-activity trifunctional fluorinated chlorosilane monomer with three reactive silicon-chlorine bonds and stable pentafluorophenylpropyl functional segments. It can undergo uniform hydrolysis and polycondensation reaction to introduce high-inertness fluorinated aromatic groups into silicone molecular chains, efficiently synthesizing high-crosslinking-density fluorosilicone resins and fluorosilico
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CHLORODIMETHYL[3-(2,3,4,5,6-PENTAFLUOROPHENYL)PROPYL]SILANE (CAS NO.157499-19-9)
1. Ultra-low Surface Energy Fluorosilicone Synthetic Monomer This product is a high-activity fluorinated aromatic chlorosilane monomer containing pentafluorophenyl functional structure and reactive Si-Cl bonds. It can undergo hydrolysis and copolymerization reaction to introduce high-stability perfluorophenyl segments into silicone molecular chains. It effectively reduces the surface energy of silicone materials and prepares high-performance fluorosilicone polymers with
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DIETHYLISOPROPYLSILYL TRIFLUOROMETHANESULFONATE (CAS NO. 126889-55-2)
1. High-Precision Silyl Protection Reagent for Complex Organic Synthesis Diethylisopropylsilyl trifluoromethanesulfonate (DEIPSOTf) is a high-activity, sterically tunable silylation reagent superior to conventional TMS and TBS protecting agents. It features moderate steric hindrance and ultra-high silylation activity, enabling highly selective protection of hydroxyl, amino and carboxyl groups in complex molecular systems under mild and anhydrous conditions. The introduced
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(2-BROMOETHOXY)-TERT-BUTYLDIMETHYLSILANE（CAS NO.86864-60-0 ）
1. Organic Synthesis Brominated Silylation Intermediate This product is a high-activity bifunctional silicon intermediate containing sterically hindered TBS protective group and reactive bromoalkyl segment. The terminal carbon-bromine bond possesses high chemical activity and can participate in nucleophilic substitution, coupling and chain extension reactions. It is widely applied in the structural derivation and functional modification of complex organic molecules,
