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(3-Chlor-4-butyrylphenoxy)essigsaeure, also known as 3-chloro-4-(butyrylphenoxy)acetic acid, is a chemical compound with the molecular formula C12H15ClO3. It is a derivative of chlorophenoxyacetic acid, featuring a chlorinated phenol group and a butyryl chain attached to the phenol ring. (3-Chlor-4-butyrylphenoxy)essigsaeure is primarily used as an intermediate in the synthesis of various agrochemicals, particularly herbicides, due to its ability to influence plant growth and development. Its chemical structure allows it to target specific enzymes or receptors in plants, making it a valuable component in the development of selective herbicides. The compound's properties, such as its solubility and stability, also play a role in its effectiveness and application in agricultural settings.

1214-82-0

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1214-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1214-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1214-82:
(6*1)+(5*2)+(4*1)+(3*4)+(2*8)+(1*2)=50
50 % 10 = 0
So 1214-82-0 is a valid CAS Registry Number.

1214-82-0Relevant 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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