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三(三甲硅烷基)硅烷

产品号 B22457 公司名称 Alfa Aesar
CAS号 1873-77-4 公司网站 http://www.alfa.com
分子式 C9H28Si4 电 话
分子量 248.66062 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 148644

产品价格信息

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产品别名

标题
Tris(trimethylsilyl)silane
IUPAC标准名
1,1,1,3,3,3-hexamethyl-2-(trimethylsilyl)trisilane
IUPAC传统名
1,1,1,3,3,3-hexamethyl-2-(trimethylsilyl)trisilane
别名
TTMSS

产品登记号

默克索引号 149757
MDL号 MFCD00077893
Beilstein号 1923953
EC号 000-000-0
CAS号 1873-77-4

产品性质

纯度 97%
沸点 82-84°C/12mm
密度 0.806
闪点 55°C(131°F)
折射率 1.4900
GHS危险品标识 GHS02
GHS危险品标识 GHS07
GHS危险声明 H226-H315-H319-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
GHS警示性声明 P210-P241-P303+P361+P353-P305+P351+P338-P405-P501A
危险公开号 10-36/37/38
安全公开号 26-37-60
保存注意事项 Light Sensitive
TSCA收录
联合国危险货物等级 3
联合国危险货物编号 UN1993
联合国危险货物包装类别(PG) II

产品详细信息

参考文献

  • Alkyl and cycloalkyl acid chlorides undergo hydrodechlorocarbonylation to hydrocarbons in high yield: Tetrahedron Lett., 33, 1787 (1992).
  • Superior to TBTH for the radical mediated cyclization of bromo lactones, avoiding the need for very high dilutions: Heterocycles, 37, 289 (1994).
  • For a brief survey of uses of this reagent in Organic synthesis, see: Synlett, 1972 (2007).
  • For a review of organosilanes as radical-based reducing agents in synthesis, see: Acc. Chem. Res., 25, 188 (1992). See also Appendix 4.
  • Radical-based reducing agent, e.g. for hydrodehalogenation reactions of halides to the corresponding hydrocarbons: J. Org. Chem., 56, 678 (1991); cf TBTH (Tri-n-butyltin hydride, A13298). Reversal of the stereoselectivity observed in the TBTH reduction of gem-dichlorides has been reported: J. Am. Chem. Soc., 116, 10781 (1994).
  • In the presence of a free-radical initiator, ring closure reactions of bromides containing a suitably-positioned double bond can be effected: Tetrahedron Lett., 38, 8165 (1997); 39, 7267 (1998). In the presence of CO, 1,5-dienes undergo tandem silylcarbonylation and cyclization to give cyclopentanone derivatives: J. Organomet. Chem., 548, 105 (1997).
  • Effects the hydrosilylation of alkenes and alkynes in high yield: J. Org. Chem., 57, 3994 (1992); this reaction forms the basis of a (Z) - (E) olefin interconversion via addition-elimination of the tris(TMS)silane radical: J. Org. Chem., 60, 3826 (1995).