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4-Hydroxy-1,6-diphenyl-pyridin-2(1H)-one is a chemical compound with the molecular formula C17H13NO2. It is a derivative of pyridin-2(1H)-one, featuring a hydroxyl group at the 4-position and two phenyl rings attached to the 1 and 6 positions. This organic molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound is characterized by its yellow crystalline appearance and is typically used as an intermediate in the preparation of more complex molecules. Its chemical properties and reactivity make it a valuable component in the field of organic chemistry, particularly in the development of new drugs and chemical compounds.

4812-99-1

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4812-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4812-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4812-99:
(6*4)+(5*8)+(4*1)+(3*2)+(2*9)+(1*9)=101
101 % 10 = 1
So 4812-99-1 is a valid CAS Registry Number.

4812-99-1Relevant articles and documents

Synthesis of Acetyl and Iodo Derivatives of 4-Hydroxy-6-phenyl-6H-pyrano[3,2-c]pyridine-2,5-diones and 4-Hydroxy-1-phenylpyridin-2(1H)-ones

Nikam,Kappe

, p. 546 - 550 (2017/02/03)

A simple and efficient method has been described for the synthesis of acetyl and iodo derivatives of 4-hydroxy-6-phenyl-6H-pyrano[3,2-c]pyridine-2,5-diones 1 and 4-hydroxy-1-phenylpyridin-2(1H)-ones 5. Compounds 1 with phenyl and alkyl substituent at C(7) and C(8), respectively, can be easily acetylated by refluxing in a mixture of acetic acid and polyphosphoric acid to give 3-acetyl-4-hydroxy-6-phenyl-6H-pyrano[3,2-c]pyridine-2,5-diones 2 in excellent yields. Compounds 1 and 5 can be iodinated with iodine and anhydrous sodium carbonate in boiling dioxane to give 4-hydroxy-3-iodo-6-phenyl-6H-pyrano[3,2-c]pyridine-2,5-diones 3 and 4-hydroxy-3-iodo-1-phenylpyridin-2(1H)-ones 6, respectively, in good yields. The structures were confirmed using infrared, nuclear magnetic resonance, and elemental analysis.

Thermal Cyclization of 3-Acyl-4-azidopyridines to Isoxazolo[4,3-c]pyridines

Stadlbauer, Wolfgang,Fiala, Werner,Fischer, Michaela,Hojas, Gerhard

, p. 33 - 39 (2007/10/03)

4-Azidopyridines such as 3-acetyl-4-azido-2-pyridones 3 or 4-azido-3-ethoxycarbonylpyridine 7 with reactive ortho-acyl substituents were obtained from the 4-hydroxy-2-pyridones 1, resp. 5 via 4-tosyloxy-2-pyridones 2 or the 2,4-dichloropyridine 6. DSC-ass

Thermal cyclization of 4-azido-3-nitropyridines to furoxanes [1]

Stadlbauer,Fiala,Fischer,Hojas

, p. 1253 - 1256 (2007/10/03)

4-Chloro-3-nitro-2-pyridines 3 and 10, obtained from 4-hydroxy-2-pyridones 1 and 8 after nitration and chlorination, gave with sodium azide 4-azido-3-nitropyridines 4 and 11, which cyclized on thermolysis to furoxans 6 and 12. Desoxygenation of the furoxa

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