"silane"
- 32 Items Found-
2-(4-ПИРИДИЛЭТИЛ)ТРИЭТОКСИСИЛАН (НОМЕР CAS 98299-74-2)
1. Functional Self-Assembled Monolayer (SAM) Precursor As a dual-functional pyridyl-modified triethoxysilane, this reagent can form highly ordered, dense and uniform self-assembled monolayer films on inorganic substrate surfaces via controlled hydrolysis and crosslinking. The surface-exposed pyridine groups provide stable chemical activity and structural regularity, which can be used for nano-surface patterning, atomic force microscope nano-shaving modification and precision
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Трихлороктадецилсилан
(CAS NO.112 -04 -9) 1. Long-chain Alkyl Silicone Polymer Synthetic Monomer This product is a high-activity trifunctional long-chain alkyl chlorosilane with three hydrolyzable Si-Cl reactive sites and stable saturated octadecyl linear alkyl segments. It can undergo uniform hydrolysis and polycondensation reaction to synthesize high-stability long-chain alkyl modified silicone resin and polysiloxane polymers. It effectively improves the lipophilicity, film-forming property and
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П-трихлоррозиллилбифенил (CAS No 18030-61-0)
1. High-refractive-index Silicone Material Synthetic Monomer This product is a high-performance aromatic chlorosilane monomer with a rigid biphenyl conjugated structure. Compared with single phenyl silane monomers, its biphenyl skeleton has higher molecular rigidity and refractive index. It can undergo hydrolysis and polycondensation to synthesize high-refractive-index silicone resin and silicone oil, which is widely used in the preparation of optical transparent silicone
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1,4-фениленбис (диметилсиланол) (Cas No.2754-32-7)
1. High-temperature Resistant Silicone Resin Synthetic Monomer This product is a rigid aromatic silicone diol monomer with a central phenylene rigid structure and double terminal reactive silanol groups. It can undergo dehydration polycondensation with silane monomers to construct high-rigidity silicone resin networks. The introduced benzene ring skeleton effectively improves the thermal decomposition temperature, thermal oxidation stability and structural rigidity of
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3- ((ETHOXYDIMETHYLSILYL) PROPAN-1-AMINE (CAS No 18306-79-1)
1. High-performance Organic-inorganic Coupling Agent This product is a bifunctional organosilane containing hydrolyzable ethoxy silyl group and active amino group. It can undergo hydrolysis and condensation reaction with hydroxyl groups on the surface of inorganic substrates such as glass, silica and metal oxides, and form chemical bonding with organic polymer matrices. It effectively optimizes interfacial compatibility and improves the comprehensive performance of composite
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(N,N-ДИМЕТИЛАМИНО)ДИМЕТИЛСИЛАН (НОМЕР CAS 22705-32-4)
1. High-efficiency Siliconization & Silylation Reagent As a highly active amino silane reagent, it contains reactive dimethylamino silyl functional groups, which can efficiently react with active hydrogen groups such as hydroxyl and carboxyl. It is widely used for silylation modification of organic compounds, polymer materials and inorganic substrate surfaces, effectively reducing surface polarity and improving chemical stability and hydrophobicity of materials. 2. Polymer
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Бутилхлородиметилсилан (CAS No 1000-50-6)
1. Functional Group Protection in Organic Synthesis As a silicon-based protecting reagent with moderate stability, butylchlorodimethylsilane compensates for the deficiencies of conventional silylating agents, including the facile hydrolysis of trimethylsilyl (TMS) groups and the high steric hindrance-induced low reactivity of tert-butyldimethylsilyl (TBS) groups. It is specially applied for the hydroxyl protection of complex natural products, pharmaceutical intermediates and
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6-Фенилгексилдиметилхлоросилан (CAS No 97451-53-1)
1. High-Precision Functional Group Protection Reagent for Organic Synthesis As an upgraded long-chain phenyl-modified silyl protecting reagent, 6-Phenylhexyldimethylchlorosilane effectively compensates for the low stability of TMS groups and excessive steric hindrance of conventional short-chain phenyl silyl reagents. The ultra-long flexible alkyl spacer significantly reduces steric hindrance, ensuring high reaction activity while introducing rigid phenyl structure to enhance
