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3-Brom-4-(2-methylen-butyryl)-phenoxyessigsaeure, also known as 3-bromo-4-(2-methylidene-butyryl)-phenoxyacetic acid, is a complex organic compound with the molecular formula C12H13BrO4. It features a phenoxyacetic acid structure, with a bromine atom at the 3-position, and a 2-methylidene-butyryl group attached at the 4-position. 3-Brom-4-<2-methylen-butyryl>-phenoxyessigsaeure is characterized by its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the production of certain chemical compounds. Due to its specific functional groups and structural features, it is of interest to researchers in the field of organic chemistry and may have implications in the development of new drugs and chemical products.

6467-28-3

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6467-28-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6467-28-3 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, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6467-28:
(6*6)+(5*4)+(4*6)+(3*7)+(2*2)+(1*8)=113
113 % 10 = 3
So 6467-28-3 is a valid CAS Registry Number.

6467-28-3Downstream Products

6467-28-3Relevant 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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