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2-(3-Chlor-4-methacryloyl-phenoxy)-propionsaeure, also known as 2-(3-chloro-4-methacryloyloxyphenoxy)propionic acid, is a chemical compound with the molecular formula C12H11ClO5. It is a derivative of propionic acid, featuring a chlorinated phenoxy group and a methacryloyl group attached to the phenol ring. 2-<3-Chlor-4-methacryloyl-phenoxy>-propionsaeure is primarily used as a reactive diluent in the production of dental composites and adhesives, where it helps to reduce the viscosity of the resin, improve the handling properties, and enhance the mechanical strength of the final product. The presence of the methacryloyl group allows it to polymerize with other components in the dental material, contributing to the formation of a stable and durable restorative material.

6467-49-8

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6467-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6467-49-8 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, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6467-49:
(6*6)+(5*4)+(4*6)+(3*7)+(2*4)+(1*9)=118
118 % 10 = 8
So 6467-49-8 is a valid CAS Registry Number.

6467-49-8Downstream Products

6467-49-8Relevant 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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