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方案
98%
折射率
n20/D 1.5486 (lit.)
沸点
142 °C/17 mmHg (lit.)
mp
18.8 °C (lit.)
密度
1.314 g/mL at 25 °C (lit.)
SMILES字符串
ClC(=O)COc1ccc(Cl)cc1
InChI
1S/C8H6Cl2O2/c9-6-1-3-7(4-2-6)12-5-8(10)11/h1-4H,5H2
InChI key
VRBVHQUSAOKVDH-UHFFFAOYSA-N
应用
4-Chlorophenoxyacetyl chloride was used in the preparation of:
- substituted acetophenone derivatives
- 2-(4-chlorophenoxyacetylamino)-3-ethoxycarbonyl[2,3-b]quinuclidine
- 2-(4-chlorophenoxy)-N′-[2-(4-chlorophenoxy)acetyl]acetohydrazide monohydrate
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
Ting Chen et al.
Acta crystallographica. Section E, Structure reports online, 66(Pt 11), o2829-o2829 (2010-01-01)
In the title compound, C(16)H(14)Cl(2)N(2)O(4)·H(2)O, the hydrazine and water mol-ecules are both located on twofold axes. The C-N-N-C torsion angle is -72.66 (1)° and the dihedral angle between the two benzene rings is 67.33 (1)°. In the crystal, mol-ecules are linked into
Synthesis and properties of 2-amino-3-ethycarbonylthieno [2, 3-b] quinuclidines.
Kaminka ME, et al.
Pharmaceutical Chemistry Journal, 21(8), 568-570 (1987)
Jonathan Rosen et al.
Organic letters, 9(4), 667-669 (2007-01-27)
A direct and efficient method was developed for the preparation of a variety of substituted acetophenone derivatives from readily available arene precursors and acid chlorides. This method has significant generality and affords access to substitution patterns on aryl rings not
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