推荐产品
质量水平
方案
98%
mp
27-29 °C (lit.)
官能团
chloro
iodo
SMILES字符串
Clc1ccc(I)cc1Cl
InChI
1S/C6H3Cl2I/c7-5-2-1-4(9)3-6(5)8/h1-3H
InChI key
NADPFZNWCQIJJW-UHFFFAOYSA-N
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一般描述
3,4-Dichloroiodobenzene undergoes Stille coupling reaction with vinyltributyltin in the presence of Pd(0)precursors to furnish styrene derivative.
应用
3,4-Dichloroiodobenzene may be used in the preparation of:
- tetrachloromethoxybiphenyls
- 1-(3,4-dichlorophenyl)-2-trimethylsilylacetylene
- 2-(3,4-dichlorocinnamyl)isoindoline-1,3-dione
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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The synthesis and structure-activity relationship analysis of a novel class of amide-based biaryl NR2B-selective NMDA receptor antagonists are presented. Some of the studied compounds are potent, selective, non-competitive, and voltage-independent antagonists of NR2B-containing NMDA receptors. Like the founding member of
The Journal of organic chemistry, 72(15), 5809-5812 (2007-06-26)
On-line monitoring of Stille reactions was performed via direct infusion electrospray ionization mass spectrometry (ESI-MS) and its tandem version (ESI-MS/MS). When operated in the positive ion mode, ESI(+)-MS was able to transfer, directly from solution to the gas phase, the
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Synthesis and properties of various poly (diphenylacetylenes) containing tert-amine moieties.
Polymer, 49(12), 2808-2816 (2008)
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