1,2-ジクロロテトラメチルジシラン

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Danger

• 危険有害性情報

  H226：引火性の液体および蒸気

  H314：重篤な皮膚の薬傷?眼の損傷

• 注意書き

  P210：熱/火花/裸火/高温のもののような着火源から遠ざ けること。－禁煙。

  P233：容器を密閉しておくこと。

  P240：容器を接地すること/アースをとること。

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

  P303+P361+P353：皮膚（または髪）に付着した場合：直ちに汚染された衣 類をすべて脱ぐこと/取り除くこと。皮膚を流水/シャワー で洗うこと。

  P305+P351+P338：眼に入った場合：水で数分間注意深く洗うこと。次にコ ンタクトレンズを着用していて容易に外せる場合は外す こと。その後も洗浄を続けること。

1,2-ジクロロテトラメチルジシラン 価格

1,2-ジクロロテトラメチルジシラン 化学特性,用途語,生産方法

• 外観

  無色～ほとんど無色透明液体

• 説明

  1,2-DICHLOROTETRAMETHYLDISILANE is a kind of widely used organic silicon intermediates and usually be used as organic silicon blocking agent in the synthesis，such as，Si-Si Compounds; Dichlorosilanes (for Polysilanes); Electroluminescence; Functional Materials; Monochlorosilanes; Reagent for High-Performance Polymer Research; Si (Classes of Silicon Compounds); Si-Cl Compounds; Silicon Compounds (for Synthesis); Synthetic Organic Chemistry; Precursors by Metal; Vapor Deposition Precursors.

• 使用

  1,2-DICHLOROTETRAMETHYLDISILANE is used as an intermediate for preparing other organical compounds. It is also used in aqueous polymer preparation as well as a laboratory reagent. 1,2-Dihydroxy-tetramethyldisilane has been synthesized by hydrolysis of 1,2-dichloro-tetramethyldisilane and characterized by IR, NMR, MS and X-ray structure analysis.

• 合成

  Tetramethyldisilane (XIV, 0.3 mmol), excess MeSiC (IV, 1.7 mmol), diglyme (0.35 ml) and n-Bu4PCI (0.02 mmol) as catalyst were placed in an NMR tube that was cooled to -196 °C (liquid nitrogen). After evacuation in vacuo the NMR tube was sealed, warmed to r.t. and the reaction course was monitored by NMR spectroscopy. Me2SiHCI III was not detected at r.t. but the disilane was chlorinated to give disilane XV (12%). Reduction of MeSiC (H-transfer from disilane XIV) yielded V in small amounts (1.2%) while target product VI was formed in nearly 40% yield (80 °C/+4 h). At 120 °C (additional 19 h) disilane XV was reduced by about a half (1 1.9% → 6.7%) to form dimethyldichlorosilane II in 13.8% yield. The catalyst remained unreacted as shown by31P-NMR spectroscopy.

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