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2-(3-Chlor-4-butyryl-phenoxy)-propionsaeure, also known as 2-(3-chloro-4-butyrylphenoxy)propionic acid, is a chemical compound with the molecular formula C12H15ClO4. It is a derivative of propionic acid, featuring a chlorinated phenoxy group attached to the propionic acid backbone. 2-<3-Chlor-4-butyryl-phenoxy>-propionsaeure is characterized by its potential applications in various chemical and pharmaceutical processes, such as the synthesis of pharmaceuticals or as an intermediate in the production of certain agrochemicals. Its specific structure, with a chlorine atom at the 3-position and a butyryl group at the 4-position of the phenoxy ring, gives it unique properties that can be exploited in these applications.

4804-87-9

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4804-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4804-87-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,0 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4804-87:
(6*4)+(5*8)+(4*0)+(3*4)+(2*8)+(1*7)=99
99 % 10 = 9
So 4804-87-9 is a valid CAS Registry Number.

4804-87-9Relevant 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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