CAS: 17869-76-0; (But-3-Yn-2-Yloxy)Trimethylsilane
该化合物是有机硅化合物,其特点是存在三组甲基硅原子,并存在由1-甲基-2-丙基-1-醇衍生的烷氧化合物.该化合物一般是一种无色液体,由于存在丙基胺而以其活性而闻名,可参与各种化学反应,包括聚合和交叉连接过程.该化合物经常用于硅基材料的合成中,并用作硅聚合物配制中的混合剂.应当参考烷氧化合物组的存在,以提高其与有机亚酸酯的兼容性,使其在表面修改和吸附应用中有用.此外,三甲基[(1-甲基-2-丙基--1-yl)氧基]硅在一定条件下可能具有诸如低挥发性和稳定性等特性,尽管应对其处理时应当注意潜在的再活性.应当参考安全数据表,以便处理和存储建议.
- 英文名称(But-3-Yn-2-Yloxy)Trimethylsilane
- 中文名称2-三甲基硅氧基-3-丁炔
- IUPAC名称(but-3-yn-2-yloxy)trimethylsilane
- 其它别名3-(Trimethylsiloxy)-1-Butyne; 3-(Trimethylsilyloxy)-1-Butyne; 2-Trimethylsiloxy-3-Butyne; 2-Trimethylsilyloxy-3-Butyne; 2-Trimethylsilyloxy-3-Butyne, 2-Trimethylsilyloxy-3-Butyne, 2-Trimethylsilyloxy-3-Butyne, ; (1-Methyl-2-Propynyl)(Trimethylsilyl) Ether; (1-Methyl-2-Propynyloxy)Trimethylsilane
- CAS编号17869-76-0
- MFCD编号:MFCD00190215
- EINECS号:625-502-2
- 分子式:C7H14OSi分子量:142.27
- 产品CID: 918960
- 产品分类化学试剂 → 硅烷试剂
物理性质
MSDS等安全信息
欧盟法规
ECHA物质C&L通报上下游产品
chloro-trimethyl-silane triethyl-(1-methyl-prop-2-ynyloxy)-stannane but-3-yn-2-ol 1,1,1,3,3,3-hexamethyl-disilazane 4-trimethylsilyl-3-butyn-2-ol (1R,4R,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,2,6-trimethyl-1-((E)-3-trimethylsilanyloxy-but-1-enyl)-cyclohexanol (1S,4R,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2,2,6-trimethyl-1-((E)-3-trimethylsilanyloxy-but-1-enyl)-cyclohexanol 1,3,5-tris(1-(trimethylsilyloxy)ethyl)benzene合成工艺路线路线简述
📜3-丁炔-2-醇置于三甲基氯硅烷体系中,用60%的收率获得2-三甲基硅氧基-3-丁炔
参考文献:Novel Acetylenic Compounds Useful As Starting Materials For Preparing An
标题:Novel Acetylenic Compounds Useful As Starting Materials For Preparing An
摘要:新型乙炔化合物,可用作制备β-单萜酮的起始材料.其制备过程和用途.
海关参考信息
- 2901292000-乙炔
2905122000-异丙醇 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:US-4661641-A
优先权日:1983-06-09
标题 :Substituted alkynes useful as intermediates in the synthesis of carotenoids
发明人：LUKAC TEODOR; SOUKUP MILAN; WIDMER ERICH
权利人:HOFFMANN LA ROCHE
摘要:Compounds of the formula ##STR1## wherein n is either 0 or 1; R 1 and R 2 is hydrogen and the other is hydrogen, hydroxy, oxo group, a protected hydroxy or protected oxo group; R 3 is hydroxy oxo group, â•?CH--CH 2 --OH, â•?CH--CHO or one of the foregoing groups where the hydroxy or oxo functions are protected; R 4 is --CO--OR 6 , --CO--R 6 , --CO--NR 6 R 7 , --CO--Cl or --SO 2 --R 6 ; R 6 is saturated or aromatic hydrocarbon; and R 7 is saturated or aromatic hydrocarbon or hydrogen, n are converted by cleavage of R 4 OH into corresponding cycloalkenes and protecting groups, if present, are hydrolyzed. n The compounds obtained are valuable intermediates in carotenoid syntheses.
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
合成参考文献
摘要:Eagle, P. A. C., Science of Synthesis, (2003) 5, 748.
摘要:Kantlehner, W., Science of Synthesis, (2005) 22, 815.
📝 需求与反馈
尽可能描述清楚需求与问题信息
