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2-(3-Chlor-4-(2-methylen-butyryl)-phenoxy)-propionsaeure, also known as 2-(3-chloro-4-(2-methylidene-butyryl)-phenoxy)-propionic acid, is a complex organic compound with the chemical formula C12H13ClO4. It is characterized by a chlorinated phenoxy group attached to a propionic acid backbone, with a 2-methylidene-butyryl substituent further modifying the phenyl ring. 2-<3-Chlor-4-(2-methylen-butyryl)-phenoxy>-propionsaeure is likely to be used in the synthesis of pharmaceuticals or agrochemicals due to its structural complexity and potential for biological activity. The presence of the chlorine atom and the unsaturated butyryl group suggests that it may have specific reactivity or properties that could be exploited in chemical reactions or as a precursor to other compounds.

6467-50-1

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6467-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6467-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6467-50:
(6*6)+(5*4)+(4*6)+(3*7)+(2*5)+(1*0)=111
111 % 10 = 1
So 6467-50-1 is a valid CAS Registry Number.

6467-50-1Downstream Products

6467-50-1Relevant 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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