135550
3,4,5,6-Tetrachlorophthalimide
97%
Synonym(s):
4,5,6,7-Tetrachloroisoindole-1,3-dione
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About This Item
Empirical Formula (Hill Notation):
C8HCl4NO2
CAS Number:
Molecular Weight:
284.91
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
mp
>300 °C (lit.)
solubility
DMF: soluble 25 mg/mL, clear, light yellow
functional group
chloro
SMILES string
Clc1c(Cl)c(Cl)c2C(=O)NC(=O)c2c1Cl
InChI
1S/C8HCl4NO2/c9-3-1-2(8(15)13-7(1)14)4(10)6(12)5(3)11/h(H,13,14,15)
InChI key
LPUUYZVKCMCHLO-UHFFFAOYSA-N
Related Categories
Application
3,4,5,6-Tetrachlorophthalimide was used to study the influence of metal binding and posttranslational modification of the carboxylated lysine on the activity of recombinant hydantoinase from Agrobacterium radiobacter.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Cheng-Yang Huang et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 14(1), 111-121 (2008-09-11)
Bacterial hydantoinase possesses a binuclear metal center in which two metal ions are bridged by a posttranslationally carboxylated lysine. How the carboxylated lysine and metal binding affect the activity of hydantoinase was investigated. A significant amount of iron was always
Mukesh C Joshi et al.
Current topics in medicinal chemistry, 20(8), 617-697 (2020-01-28)
The side-chains of quinoline antimalarial agents are the major concern of focus to build novel and efficaciaous bioactive and clinical antimalarials. Bioative antimalarial analogs may play a critical role in pH trapping in the food vacuole of RBC's with the
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