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135550

Sigma-Aldrich

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:
1571-13-7
Molecular Weight:
284.91
EC Number:
216-386-0
MDL number:
MFCD00005883
UNSPSC Code:
12352100
PubChem Substance ID:
24848209
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

>300 °C (lit.)

solubility

DMF: soluble 25 mg/mL, clear, light yellow

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

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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