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Propionic acid 1,2-dihydro-6-methyl-2-oxopyridin-4-yl ester is a chemical compound with the molecular formula C10H13NO3. It is an ester derivative of propionic acid, where the hydroxyl group of the acid is replaced by a 1,2-dihydro-6-methyl-2-oxopyridin-4-yl group. Propionic acid 1,2-dihydro-6-methyl-2-oxopyridin-4-yl ester is characterized by its aromatic structure, which includes a pyridine ring with a methyl group at the 6-position and a carbonyl group at the 2-position. It is a white crystalline solid and is soluble in organic solvents. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity and reactivity. Its specific applications may vary, but it is often involved in the formation of complex molecules that can interact with biological targets.

7135-82-2

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7135-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7135-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7135-82:
(6*7)+(5*1)+(4*3)+(3*5)+(2*8)+(1*2)=92
92 % 10 = 2
So 7135-82-2 is a valid CAS Registry Number.

7135-82-2Downstream Products

7135-82-2Relevant 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.

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