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1,6-Dimethyl-3-acetyl-4-hydroxypyridine-2(1H)-one is a complex organic compound with the molecular formula C10H11NO2. It is a derivative of pyridine, a heterocyclic aromatic compound containing a nitrogen atom in a six-membered ring. This specific compound features two methyl groups at the 1st and 6th positions, an acetyl group (a two-carbon acyl group) at the 3rd position, and a hydroxyl group at the 4th position. The compound exhibits a 2(1H)-one functional group, indicating the presence of a ketone group. Due to its unique structure, it has potential applications in various fields, such as pharmaceuticals and agrochemicals, as a building block for the synthesis of more complex molecules.

7202-55-3

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7202-55-3 Usage

Chemical structure

Pyridine derivative with two methyl groups, an acetyl group, and a hydroxy group

Methyl groups

Attached to the 3 and 6 positions

Acetyl group

Attached to the 3 position

Hydroxy group

Attached to the 4 position

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Potential properties

Neuroprotective and antioxidant

Therapeutic applications

Treating neurodegenerative diseases and oxidative stress-related disorders

Additional applications

Organic synthesis and medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 7202-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7202-55:
(6*7)+(5*2)+(4*0)+(3*2)+(2*5)+(1*5)=73
73 % 10 = 3
So 7202-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO3/c1-5-4-7(12)8(6(2)11)9(13)10(5)3/h4,13H,1-3H3

7202-55-3Relevant academic research and scientific papers

Synthesis of functionalized pyrano[3,2-c]pyridines and their transformations to 4-hydroxy-3[(1E)-N-hydroxyalkanimidoyl]pyridones

El-Essawy, Farag A.,Khattab, Ahmed F.,Zahran, Magdy A.,Gomaa, Sherif H.

, p. 3225 - 3237 (2008/02/12)

Reaction of 4-hydroxy-6-methyl-2(1H)-pyridones 1a and 4-hydroxy-1,6- dimethyl-2(1H)-pyridones 1b with diethyl malonates 2a-e leads to the formation of pyrano[3,2-c]pyridines 4a-j. Degradation of 4a-i affords the corresponding ketones 6a-i. Condensation of ketones 6a-i with hydroxyl amine or phenyl hydrazine hydrochloride is described. Copyright Taylor & Francis Group, LLC.

Ring closure of 4-azido-3-formyl-(or acetyl-)2-pyridones to isoxazolo[4,3-c]pyridones

Khattab, Ahmed F.

, p. 393 - 395 (2007/10/03)

Azidation of the chlor aldehyde 2, which was obtained from the 4-hydroxy-2-pyridone 1, afforded the ring-closed isoxazolopyridone 3. Thermolysis of the 3-acetyl-4-azido-2-pyridone 8, which was obtained from the corresponding 4-tosyloxy derivative 7, affor

REACTION OF ETHYL β-ALKYLAMINOCROTONATES IN THE PRESENCE OF ORGANIC ACID

Yamato, Masatoshi,Sato, Koichi,Hashigaki, Kuniko,Ninomiya, Mayumi

, p. 1263 - 1268 (2007/10/02)

Condensation of ethyl β-alkylaminocrotonates, obtained from ethyl acetoacetate and amines, in the presence of 3-mercaptopropionic acid gave 1,6-naphthyridine-2,5-dione derivatives.The structures of these compounds were determined on the basis of several i

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