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3-Methyl-4-(2-methylen-butyryl)-phenoxyessigsaeure, also known as 3-methyl-4-(2-methylen-butyryl)-phenoxyacetic acid, is a complex organic compound with the chemical formula C14H18O4. It is characterized by a phenoxyacetic acid structure, where the phenyl ring is substituted with a methyl group at the 3rd position and a 2-methylen-butyryl group at the 4th position. The 2-methylen-butyryl group is a derivative of butyric acid with a double bond between the second and third carbon atoms, and an additional methyl group on the second carbon. 3-Methyl-4-(2-methylen-butyryl)-phenoxyessigsaeure is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals. Its specific applications and properties would depend on its reactivity and stability, which are not detailed in this summary.

1148-36-3

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1148-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1148-36-3 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 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1148-36:
(6*1)+(5*1)+(4*4)+(3*8)+(2*3)+(1*6)=63
63 % 10 = 3
So 1148-36-3 is a valid CAS Registry Number.

1148-36-3Downstream Products

1148-36-3Relevant 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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