所有图片(3)
(E)-1,2-Bis(tributylstannyl)ethane, (E)-1,2-Bis(tributylstannyl)ethylene, (E)-1,2-Bis(tributyltin)ethylene, (E)-1,2-Ethenediylbis[tributylstannane], (E)-Bis(tributylstannyl)ethene, 1,2-Ethenediylbis[tributylstannane], trans-1,2-Bis(tributylstannyl)ethylene, trans-Bis(tributylstannyl)ethene, trans-Bis(tributylstannyl)ethylene
C26H56Sn2
推荐产品
检测方案
97%
形式
liquid
折射率
n20/D 1.502
密度
1.132 g/mL at 25 °C
储存温度
2-8°C
SMILES字符串
CCCC[Sn](CCCC)(CCCC)\C=C\[Sn](CCCC)(CCCC)CCCC
InChI
1S/6C4H9.C2H2.2Sn/c6*1-3-4-2;1-2;;/h6*1,3-4H2,2H3;1-2H;;
InChI key
VNKOWRBFAJTPLS-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
trans-1,2-Bis(tributylstannyl)ethene can be used to prepare:
- Polyarylenevinylene polymers having triphenylamine core moieties.
- Two (E)-2-(2-(thiophen-2-yl)vinyl)thiophen based copolymers through Pd-catalyzed Stille coupling reaction.
- Vinylstannanes by reacting with aryl halides, which in turn can be used in the synthesis of substituted pyridines.
警示用语:
Danger
危险分类
Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT RE 1
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Tuning optical and electronic properties of poly (4, 4′-triphenylamine vinylene) s by post-modification reactions
Dyes and Pigments, 113, 227-238 (2015)
A novel strategy for the synthesis of 2-arylpyridines using one-pot 6π-azaelectrocyclization
Tetrahedron Letters, 49(28), 4349-4351 (2008)
Synthesis, characterization, and field-effect properties of (E)-2-(2-(thiophen-2-yl) vinyl) thiophen-based donor-acceptor copolymers
Polymer, 68, 302-307 (2015)
Chemistry (Weinheim an der Bergstrasse, Germany), 26(13), 2869-2882 (2019-11-16)
A reliable synthetic protocol toward a series of fused chalcogenopheno[1]benzochalcogenophene (CBC) building blocks was developed based on a Fiesselmann reaction. The obtained CBC units were applied in McMurry and Stille coupling reactions toward symmetric regioisomeric ene-linked dimers. These π-conjugated compounds
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