所有图片(2)
别名:
3-三甲硅基丙炔酸
线性分子式:
(CH3)3SiC≡CCO2H
CAS号:
分子量:
142.23
Beilstein:
1755674
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
检测方案
98%
bp
105-110 °C/10 mmHg (lit.)
mp
47-49 °C (lit.)
SMILES字符串
C[Si](C)(C)C#CC(O)=O
InChI
1S/C6H10O2Si/c1-9(2,3)5-4-6(7)8/h1-3H3,(H,7,8)
InChI key
IPEATTYBFBRNEB-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
3-(Trimethylsilyl)propynoic acid (3-(Trimethylsilyl)propiolic acid) may be used as starting reagent for the synthesis of 3-trimethylsilylpropynamides.
3-(Trimethylsilyl)propynoic acid may be used in the regioselective preparation of 1,5-trisubstituted 1H-1,2,3-triazoles.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
One-Pot Synthesis of 3-(Trimethylsilyl) propynamides.
Medvedeva AS, et al.
Russ. J. Org. Chem., 46(10), 1466-1470 (2010)
Steven J Coats et al.
Organic letters, 7(8), 1469-1472 (2005-04-09)
[reaction: see text] A regioselective method for the preparation of 1,5-trisubstituted 1H-1,2,3-triazoles via a 1,3-dipolar cycloaddition of 1-trimethylsilylacetylenes with organoazides is described. Immobilization of the azide on REM resin and subsequent cycloaddition afforded a 2 x 2 x 4 x
Yevgen Matviychuk et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 319, 106814-106814 (2020-09-20)
Low-cost, user-friendly benchtop NMR instruments are often touted as a "one-click" solution for data acquisition, however insufficient peak dispersion in their spectra often reduces the accuracy of quantification and requires user expertise with sophisticated processing tools. Our work aims to
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门