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1192343-89-7

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1192343-89-7 Usage

Structure

A derivative of benzene with two chlorine atoms, one iodine atom, and a methyl group attached to different carbon atoms.

Functional groups

Chlorine atoms, iodine atom, and a methyl group.

Applications

Primarily used as an intermediate in the synthesis of other organic compounds, with potential applications in pharmaceuticals and agrochemicals.

Hazardous nature

Considered hazardous and may have harmful effects if it comes into contact with the skin, eyes, or respiratory system.

Safety precautions

Handle with care and use appropriate protective equipment to minimize exposure risks.

Check Digit Verification of cas no

The CAS Registry Mumber 1192343-89-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,3,4 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1192343-89:
(9*1)+(8*1)+(7*9)+(6*2)+(5*3)+(4*4)+(3*3)+(2*8)+(1*9)=157
157 % 10 = 7
So 1192343-89-7 is a valid CAS Registry Number.

1192343-89-7Downstream Products

1192343-89-7Relevant articles and documents

3-Substituted phenylalanines as selective AMPA- and kainate receptor ligands

Szymanska, Ewa,Pickering, Darryl S.,Nielsen, Birgitte,Johansen, Tommy N.

, p. 6390 - 6401 (2011/03/17)

On the basis of X-ray structures of ionotropic glutamate receptor constructs in complex with amino acid-based AMPA and kainate receptor antagonists, a series of rigid as well as flexible biaromatic alanine derivatives carrying selected hydrogen bond acceptors and donors have been synthesized in order to investigate the structural determinants for receptor selectivity between AMPA and the GluR5 subtype of kainate receptors. Compounds selective for either GluR5 or AMPA receptors were identified. One particular substituent position appeared to be of special importance for control of ligand selectivity. Using molecular modeling the observed structure-activity relationships at AMPA and GluR5 receptors were deduced.

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