クロロトリス(フェニルメチル)シラン
トリベンジルシリルクロリド · クロロトリス(フェニルメチル)シラン · トリベンジル(クロロ)シラン · CHLOROTRIBENZYLSILANE · TRIBENZYL CHLOROSILANE · TRIBENZYLSILYL CHLORIDE · tribenzylchlorosilicane · Tribenzylchlorosilane 97%

識別子と物理属性
| CAS No. | 18740-59-5 |
|---|---|
| 分子式 | C21H21ClSi |
| 平均分子量 | 336.9 g/mol |
| 単同位体質量 | 336.11010488 g/mol |
| SMILES | Cl[Si](Cc1ccccc1)(Cc1ccccc1)Cc1ccccc1 |
| InChIKey | UTXPCJHKADAFBB-UHFFFAOYSA-N |
| PubChem CID | 87774 |
| EC No. | 242-549-0 |
| DTXSID | DTXSID0066404 |
| 現地名 | クロロトリス(フェニルメチル)シラン |
化学・物理的性質
| 極性表面積 | 0 |
|---|---|
| 水素結合供与体数 | 0 |
| 水素結合受容体数 | 0 |
| 回転可能結合数 | 6 |
| 重原子数 | 23 |
| 形式電荷 | 0 |
| 複雑度 | 274 |
| 融点 | 139-142 °C(lit.) |
| 沸点 | 437.9±14.0 °C(Predicted) |
| 密度 | 1.096±0.06 g/cm3(Predicted) |
| 溶解度 | 冷たい石油エーテルにわずかに溶け、熱い石油エーテルに中程度に溶ける。 |
| EPAの化学物質情報 | Silane, chlorotris(phenylmethyl)- (18740-59-5) |
安全性と法規制
| GHS 分類 | DangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P260, P264, P264+P265, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P321, P363, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 39 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies. |
|---|---|
| Hazard Classes and Categories | Skin Corr. 1B (100%) |
| F | 10-21 |
| 水環境危害等級(WGK) | 3 |
| TSCA 収載状態 | TSCA listed |
| 輸送番号(UN) | UN 3261 8/PG 2 |
| 危険文句(R) | 34 |
| 危険表示 | C |
| 安全措置(S) | 26-36/37/39-45 |
| 危険等級 | 8 |
| 包装等級 | II |
用途
使用
Tribenzylchlorosilane is widely used as reagent for alcohol protection.
製法・合成法
製造方法
It is prepared by reaction of benzylmagnesium chloride with SiCl4 in ether; separation from mono- and dibenzylated chlorosilane byproducts is then accomplished by fractional distillation (boiling range 300–360 °C/100 mmHg). Other preparations involve the chlorination of tribenzylsilane using Cl2 or an acyl chloride. No yields are reported for any of the above preparative procedures.
純化方法
It is recrystallised three times from pet ether (in slender colourless needles, m 141o). It is sparingly soluble in pet ether but is soluble in Et2O. It does not fume in moist air but is decomposed by H2O to give tribenzyl silanol m 106o (from pet ether). [Robinson & Kipping J Chem Soc 93 439 1908, Jenkins & Post J Org Chem 15 556 1950, Beilstein 16 H 906, 16 IV 1498.]