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1-(4-Hydroxy-2,3-dimethyl-phenyl)-butan-1-one, also known as 4-hydroxy-2,3-dimethylacetophenone, is an organic compound with the molecular formula C11H14O2. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents and has a melting point of 47-49°C. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a fragrance ingredient in the perfume industry due to its pleasant aroma. The compound is synthesized through various methods, including the Friedel-Crafts acylation of 2,3-dimethylphenol with acetic anhydride, followed by hydrolysis and oxidation. It is important to handle this chemical with care, as it may cause skin and eye irritation, and prolonged exposure may lead to respiratory issues.

5862-05-5

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5862-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5862-05-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,6 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5862-05:
(6*5)+(5*8)+(4*6)+(3*2)+(2*0)+(1*5)=105
105 % 10 = 5
So 5862-05-5 is a valid CAS Registry Number.

5862-05-5Relevant academic research and scientific papers

Inhibitory effects of ethacrynic acid analogues lacking the α,β-unsaturated carbonyl unit and para-acylated phenols on human cancer cells

Bryant, Zack E.,Janser, Romy F.J.,Jabarkhail, Medina,Candelaria-Lyons, Melissa S.,Romero, Brittni B.,Slambrouck, Severine Van,Steelant, Wim F.A.,Janser, Ingo

scheme or table, p. 912 - 915 (2011/03/21)

A series of ethacrynic acid analogues, lacking the α,β- unsaturated carbonyl unit, was synthesized and subsequently evaluated for their ability to inhibit the migration of human breast cancer cells, Hs578Ts(i)8 as well as of human prostate cancer cells, C4-2B. These cell lines provide a good model system to study migration and invasion, since they represent metastatic cancer. Our studies show that ethacrynic acid analogues with methyl substituents at the aromatic ring demonstrate no inhibitory effect on the migration of both cancer cell lines, whereas a precursor in the synthesis of these ethacrynic acid analogues (II-1, a para-acylated m-cresol) is an excellent inhibitor of the migration of both cancer cell lines.

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