731528
trans-2-Ethoxyvinylboronic acid pinacol ester
95%
别名:
(E)-2-(2-Ethoxyvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, (E)-2-Ethoxyvinylboronic acid pinacol ester
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C10H19BO3
化学文摘社编号:
分子量:
198.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
InChI
1S/C10H19BO3/c1-6-12-8-7-11-13-9(2,3)10(4,5)14-11/h7-8H,6H2,1-5H3/b8-7+
SMILES string
CCO\C=C\B1OC(C)(C)C(C)(C)O1
InChI key
MRAYNLYCQPAZJN-BQYQJAHWSA-N
assay
95%
form
liquid
refractive index
n20/D 1.447
density
0.935 g/mL at 25 °C
functional group
ether
storage temp.
2-8°C
Quality Level
Application
trans-2-Ethoxyvinylboronic acid pinacol ester is a boronic ester commonly used in Suzuki-Miyaura cross-coupling.
This reaction is a key step to synthesize:
This reaction is a key step to synthesize:
- Azaindole and diazaindoles from chloroamino-N-heterocycles.
- Doryanine and its derivatives from 2-bromobenzoic acid.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
188.1 °F
flash_point_c
86.7 °C
法规信息
新产品
此项目有
Total Synthesis of the Illicium-Derived Sesquineolignan Simonsol C.
Nugent, Jeremy et al.
Organic Letters, 18(15), 3798-3801 (2016)
Two-step synthesis of aza-and diazaindoles from chloroamino-N-heterocycles using ethoxyvinylborolane.
Whelligan, Daniel K et al.
The Journal of Organic Chemistry, 75(1), 11-15 (2009)
Efficient and rapid synthesis of N-substituted isoquinolin-1-ones under mild conditions: Facile access to doryanine derivatives
Takwale AD, et al.
Tetrahedron Letters, 60(18), 1259-1261 (2019)
Structure-and reactivity-based development of covalent inhibitors of the activating and gatekeeper mutant forms of the epidermal growth factor receptor (EGFR).
Ward, Richard A et al.
Journal of Medicinal Chemistry, 56(17), 7025-7048 (2013)
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.
联系客户支持