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| | CHLOROPHENYLTRIETHOXYSILANE Basic information |
| Product Name: | CHLOROPHENYLTRIETHOXYSILANE | | Synonyms: | p-chlorophenyltriethoxysilane7%;p-chlorophenyltrimethoxysilane;Silane, (4-chlorophenyl)triethoxy-;(4-chlorophenyl)triethoxy-silan;(4-chlorophenyl)triethoxy-Silane;CHLOROPHENYLTRIETHOXYSILANE;Chlorophenyltriethoxysilane(mixed m.p isomers);1-CHLORO-4-TRIETHOXYSILYLBENZENE | | CAS: | 21700-74-3 | | MF: | C12H19ClO3Si | | MW: | 274.82 | | EINECS: | 244-533-9 | | Product Categories: | | | Mol File: | 21700-74-3.mol |  |
| | CHLOROPHENYLTRIETHOXYSILANE Chemical Properties |
| Melting point | <0°C | | Boiling point | 82-84 °C0.07 mm Hg(lit.) | | density | 1.069 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.474(lit.) | | Fp | >230 °F | | Specific Gravity | 1.08 | | Hydrolytic Sensitivity | 7: reacts slowly with moisture/water | | EPA Substance Registry System | Silane, (4-chlorophenyl)triethoxy- (21700-74-3) |
| | CHLOROPHENYLTRIETHOXYSILANE Usage And Synthesis |
| Uses | (4-Chlorophenyl)triethoxysilane can be used:
- To facilitate the connection between dipolar mixed monolayers and?zinc oxide in photovoltaic devices.
- As a substrate in the Ni-catalyzed decarboxylative coupling with alkynyl carboxylic acids to yield substituted diarylalkynes.
- As a substrate in the Hiyama cross-coupling reactions with 3-iodoazetidines to yield substituted 3-arylazetidines.
- As an intermediate in the synthesis of tripod-shaped oligo(p-phenylene)s, which are used in the surface immobilization of gold and CdS quantum dots for sensor applications.
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| | CHLOROPHENYLTRIETHOXYSILANE Preparation Products And Raw materials |
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