推荐产品
方案
97%
折射率
n20/D 1.618 (lit.)
密度
1.72 g/mL at 25 °C (lit.)
SMILES字符串
CC(=O)c1ccccc1I
InChI
1S/C8H7IO/c1-6(10)7-4-2-3-5-8(7)9/h2-5H,1H3
InChI key
XDXCBCXNCQGZPG-UHFFFAOYSA-N
一般描述
2′-Iodoacetophenone is a halogenated aromatic ketone.
应用
2′-Iodoacetophenone (2-Iodoacetophenone) may be used in the synthesis of:
- indene derivatives
- di-(o-acetylphenyl)acetylene
- indenol derivative
储存分类代码
12 - Non Combustible Liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
Kuo-Jui Chang et al.
The Journal of organic chemistry, 69(14), 4781-4787 (2004-07-03)
An efficient cobalt-catalyzed carbocylization for the synthesis of indenols and indenes and a new method for reductive decyanation are described. 2-Iodophenyl ketones and aldehydes 1a-g undergo carbocyclization with various disubstituted alkynes 2a-k in the presence of Co(dppe)I(2) and zinc powder
Charles P Casey et al.
Beilstein journal of organic chemistry, 1(1), 18-18 (2006-03-18)
The reaction of di-(o-acetylphenyl)acetylene (1) with excess dimethyl acetylenedicarboxylate (DMAD) produced bis-DMAD adducts meso-3 and rac-3. This transformation is suggested to involve thermal rearrangement of 1 to the intermediate 3,3'-dimethyl-1,1'-biisobenzofuran (A), and subsequent Diels-Alder cycloadditions of two equivalents of DMAD
Cobalt-Catalyzed Carbocyclization of o-Iodobenzaldehydes and o-Iodophenylketones with Alkynes.
Chang KJ, et al.
Organic Letters, 5(21), 3963-3966 (2003)
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