Tris(trimethylsilyl)silane

B. Giese, J. Dickhaut, C. Chatgilialoglu
{"title":"Tris(trimethylsilyl)silane","authors":"B. Giese, J. Dickhaut, C. Chatgilialoglu","doi":"10.1002/9780470842898.RT420.PUB2","DOIUrl":null,"url":null,"abstract":"[1873-77-4] C9H28Si4 (MW 248.73) \n \n \n \n \n \nInChI = 1S/C9H28Si4/c1-11(2,3)10(12(4,5)6)13(7,8)9/h10H,1-9H3 \n \n \n \nInChIKey = SQMFULTZZQBFBM-UHFFFAOYSA-N \n \n \n \n(mediator of radical reactions;1, 2 nontoxic substitute for tri-n-butylstannane in radical reactions; slower hydrogen donor than tri-n-butylstannane3) \n \n \n \nAlternatives names: TTmss(Tms)3SiH \n \n \n \nPhysical Data: bp 82–84 °C/12 mmHg; d 0.806 g cm−3; n20D 1.489. \n \n \n \nSolubility: sol pentane, ether, toluene, THF; modestly sol acetone, acetonitrile; insol H2O; decomposes rapidly in methanol and other alcohols. \n \n \n \nForm Supplied in: colorless liquid; commercially available. \n \n \n \nPreparative Method: easy to synthesize.4 \n \n \n \nHandling, Storage, and Precautions: is slightly sensitive to oxygen and should be stored under nitrogen.5 It showed no toxicity in several biological test systems.6","PeriodicalId":11669,"journal":{"name":"Encyclopedia of Reagents for Organic Synthesis","volume":"56 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2003-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Encyclopedia of Reagents for Organic Synthesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/9780470842898.RT420.PUB2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

[1873-77-4] C9H28Si4 (MW 248.73) InChI = 1S/C9H28Si4/c1-11(2,3)10(12(4,5)6)13(7,8)9/h10H,1-9H3 InChIKey = SQMFULTZZQBFBM-UHFFFAOYSA-N (mediator of radical reactions;1, 2 nontoxic substitute for tri-n-butylstannane in radical reactions; slower hydrogen donor than tri-n-butylstannane3) Alternatives names: TTmss(Tms)3SiH Physical Data: bp 82–84 °C/12 mmHg; d 0.806 g cm−3; n20D 1.489. Solubility: sol pentane, ether, toluene, THF; modestly sol acetone, acetonitrile; insol H2O; decomposes rapidly in methanol and other alcohols. Form Supplied in: colorless liquid; commercially available. Preparative Method: easy to synthesize.4 Handling, Storage, and Precautions: is slightly sensitive to oxygen and should be stored under nitrogen.5 It showed no toxicity in several biological test systems.6
三(三甲基硅烷基)硅烷
[1873-77-4] C9H28Si4 (MW 248.73) InChI = 1S/C9H28Si4/c1-11(2,3)10(12(4,5)6)13(7,8)9/h10H,1- 9h3 InChIKey = SQMFULTZZQBFBM-UHFFFAOYSA-N(自由基反应介质)替代名称:TTmss(Tms)3SiH物理数据:bp 82-84°C/12 mmHg;D 0.806 g cm−3;n20D 1.489。溶解度:溶胶戊烷、醚、甲苯、四氢呋喃;适度溶胶丙酮、乙腈;insol水;在甲醇和其它醇中迅速分解。供应形式:无色液体;商业上可用。3 .制备方法:制备简便处理、储存及注意事项:对氧气略敏感,应在氮气下储存在几种生物试验系统中均无毒性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信