所有图片(1)
别名:
5-氯-1H-吲哚-2,3-二酮
经验公式（希尔记法）:
C8H4ClNO2
CAS号:
分子量:
181.58
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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检测方案
97%
mp
254-258 °C (lit.)
SMILES字符串
Clc1ccc2NC(=O)C(=O)c2c1
InChI
1S/C8H4ClNO2/c9-4-1-2-6-5(3-4)7(11)8(12)10-6/h1-3H,(H,10,11,12)
InChI key
XHDJYQWGFIBCEP-UHFFFAOYSA-N
一般描述
5-Chloroisatin reacts with substituted 4-amino-4,5-dihydro-1H-1,2,4-triazole-5-ones to yield Schiff bases.
应用
5-Chloroisatin was used in synthesis of Schiff base by reaction with 2-methyl-4-nitroaniline.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
Olcay Bekircan et al.
Molecules (Basel, Switzerland), 13(9), 2126-2135 (2008-10-03)
Ethyl imidate hydrochlorides 1 were prepared by passing HCl gas through solutions of substituted benzyl cyanides and absolute ethanol. Ethoxycarbonylhydrazones 2 were synthesized from the reaction of compounds 1 with ethyl carbazate. Treatment of 2 with hydrazine hydrate leads to
Synthesis, Characterization and Biological Activities of a New 5-Chloroisatin Schiff Base and its Metal Complexes.
RAO R, et al.
Chemical Science Transactions, 2(3), 1063-1069 (2013)
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