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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
216-386-0
MDL number:
Assay:
97%
InChI key
LPUUYZVKCMCHLO-UHFFFAOYSA-N
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)
SMILES string
Clc1c(Cl)c(Cl)c2C(=O)NC(=O)c2c1Cl
assay
97%
mp
>300 °C (lit.)
solubility
DMF: soluble 25 mg/mL, clear, light yellow
functional group
chloro
Quality Level
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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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