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Merck
CN

901223

Sigma-Aldrich

3-(Trimethylsilyl)propargyl methacrylate

≥98.0%, contains 200 ppm MEHQ as inhibitor

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经验公式(希尔记法):
C10H16O2Si
分子量:
196.32
MDL编号:
UNSPSC代码:
12162002

检测方案

≥98.0%

形式

liquid

包含

200 ppm MEHQ as inhibitor

颜色

colorless to pale yellow

运输

wet ice

储存温度

−20°C

一般描述

3-(Trimethylsilyl)propargyl methacrylate is a methacrylate-based monomer for use in the synthesis of alkyne-functionalized polymers and copolymers. The incorporation of alkynes allows for rapid post-polymerization modification through reactions, such as copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) or thiol-yne click reactions. These reactions are highly preferable for functionalization due their high efficiency and the ability to easily install the corresponding functionality (e.g., azides or thiols) onto the biomolecule or small molecule of interest. While alkynes offer great promise for post-polymerization functionalization, it is difficult to polymerize bifunctional, alkyne-containing monomers without the synthesis of branched or highly gelled products. 3-(Trimethylsilyl)propargyl methacrylate features a silyl-protected alkyne that can be easily deprotected post-polymerization to yield alkyne-functionalized polymers and copolymers.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

闪点(°F)

193.1 °F

闪点(°C)

89.5 °C

法规信息

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Vincent Ladmiral et al.
Journal of the American Chemical Society, 128(14), 4823-4830 (2006-04-06)
The synthesis of novel well-defined alkyne side chain functional polymers featuring narrow molecular weight distributions (PDI = 1.09-1.17) by living radical polymerization is described. Grafting of protected and unprotected carbohydrates is achieved via either a C-6 or an anomeric azide
Graft block copolymers of propargyl methacrylate and vinyl acetate via a combination of RAFT/MADIX and click chemistry: Reaction analysis.
Quemener, D. et al
Journal of Polymer Science Part A: Polymer Chemistry, 46, 155-173 (2008)
Clickable initiators, monomers and polymers in controlled radical polymerizations?a prospective combination in polymer science.
Mansfeld, U. et al
Polym. Chem., 1, 1560-1598 (2010)

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