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5-(4-chlorophenyl)-5-ethylimidazolidine-2,4-dione is a chemical compound with the molecular formula C11H12ClNO2. It is a white crystalline solid that belongs to the class of imidazolidine-2,4-dione derivatives. 5-(4-chlorophenyl)-5-ethylimidazolidine-2,4-dione features a 4-chlorophenyl group attached to the imidazolidine ring, which is also substituted with an ethyl group. It is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a precursor in the synthesis of various biologically active molecules. The compound's structure and properties make it a versatile building block in the development of new drugs and pesticides.

6308-24-3

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6308-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6308-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6308-24:
(6*6)+(5*3)+(4*0)+(3*8)+(2*2)+(1*4)=83
83 % 10 = 3
So 6308-24-3 is a valid CAS Registry Number.

6308-24-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-chlorophenyl)-5-ethylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:6308-24-3 SDS

6308-24-3Downstream Products

6308-24-3Relevant academic research and scientific papers

Solvent effects on the absorption spectra of potentially pharmacologically active 5-alkyl-5-arylhydantoins: A structure-property relationship study

Hmuda, Sleem F.,Banjac, Nebojsa R.,Trisovic, Nemanja P.,Bozic, Bojan D.,Valentic, Natasa V.,Uscumlic, Gordana S.

, p. 627 - 637 (2013/07/26)

To obtain insight into the interactions of potential anticonvulsant drugs with their surrounding, two series of 5-methyl-5-aryl- and 5-ethyl-5- -arylhydantoins were synthesized and their absorption spectra were recorded in the region from 200 to 400 nm in a set of selected solvents. The effects of solvent dipolarity/polarizability and solvent-solute hydrogen bonding interactions on the absorption maxima shifts were analyzed by means of the linear solvation energy relationship (LSER) concept of Kamlet and Taft. The ratio of the contributions of specific and non-specific solvent-solute interactions were correlated with the corresponding absorption, distribution, metabolism, and excretion (ADME) properties of the studied compounds. The correlation equations were combined with different physicochemical parameters to generate new equations, which demonstrate the reasonable relationships between the solvent- solute interactions and the structure-activity parameters. Copyright (C)2013 SCS.

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