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2-(3-Chlor-4-propionyl-phenoxy)-propionsaeure, also known as 2-(3-chloro-4-propionylphenoxy)propanoic acid, is a chemical compound with the molecular formula C12H13ClO5. It is a derivative of propionic acid, featuring a chlorinated and propionylated phenoxy group attached to the second carbon of the propionic acid backbone. 2-<3-Chlor-4-propionyl-phenoxy>-propionsaeure is characterized by its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of various active ingredients. Its structure allows for the exploration of its properties and reactivity, which can be crucial in the development of new compounds with specific therapeutic or pesticidal effects.

6618-62-8

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6618-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6618-62-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6618-62:
(6*6)+(5*6)+(4*1)+(3*8)+(2*6)+(1*2)=108
108 % 10 = 8
So 6618-62-8 is a valid CAS Registry Number.

6618-62-8Relevant academic research and scientific papers

The synthesis of α,β-unsaturated carbonyl derivatives with the ability to inhibit both glutathione S-transferase P1-1 activity and the proliferation of leukemia cells

Zhao, Guisen,Liu, Chuan,Wang, Rui,Song, Dandan,Wang, Xiaobing,Lou, Hongxiang,Jing, Yongkui

, p. 2701 - 2707 (2008/02/07)

Ethacrynic acid (EA), an α,β-unsaturated carbonyl compound, is a glutathione S-transferase P1-1 (GSTP1-1) inhibitor. Twenty-one novel EA derivatives have been synthesized. The effects of these compounds on GSTP1-1 activity and on the proliferation of human leukemia HL-60 cells have been determined. Compounds with a halogen substitution at the 3′-position of the aromatic ring have greater inhibitory effects on GSTP1-1 activity than those of compounds with a methyl substitution there. Compounds with substitutions at both the 2′- and 3′-positions of the aromatic ring have more antiproliferative ability than those with one substitution at 3′-position. Esterification of the carboxyl group appears to increase the antiproliferative ability.

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