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3-Methyl-4-butyryl-phenoxyessigsaeure, also known as 3-methyl-4-(butanoyloxy)benzoic acid, is a chemical compound with the molecular formula C12H16O4. It is a derivative of benzoic acid, featuring a methyl group at the 3rd carbon, a butyryl (butanoyl) group at the 4th carbon, and a phenoxy group attached to the benzene ring. This organic compound is characterized by its potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. The compound's properties, such as its solubility and stability, can be influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

1144-57-6

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1144-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1144-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1144-57:
(6*1)+(5*1)+(4*4)+(3*4)+(2*5)+(1*7)=56
56 % 10 = 6
So 1144-57-6 is a valid CAS Registry Number.

1144-57-6Relevant 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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