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N-(2,6-dimethylphenyl)-2-hydroxy-2-phenylacetamide is a complex organic compound with the molecular formula C17H17NO2. It is a derivative of acetamide, featuring a 2,6-dimethylphenyl group attached to the nitrogen atom, a hydroxyl group, and a phenyl group on the acetamide backbone. This chemical is known for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various drugs. Its structure endows it with unique chemical properties, making it a valuable component in the development of new medications. The compound's specific role in pharmaceuticals can vary, but it is often involved in the creation of compounds that target specific receptors or enzymes in the body, highlighting its importance in the field of medicinal chemistry.

1464-80-8

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1464-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1464-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1464-80:
(6*1)+(5*4)+(4*6)+(3*4)+(2*8)+(1*0)=78
78 % 10 = 8
So 1464-80-8 is a valid CAS Registry Number.

1464-80-8Downstream Products

1464-80-8Relevant academic research and scientific papers

A Mild and Chemoselective Hydrosilylation of α-Keto Amides by Using a Cs2CO3/PMHS/2-MeTHF System

Kumar, Govindharaj,Muthukumar, Alagesan,Sekar, Govindasamy

, p. 4883 - 4890 (2017/09/13)

A Cs2CO3-catalyzed hydrosilylation reaction of α-keto amides that proceeds through the in situ formation of MeSiH3 has been developed by using inexpensive polymethylhydrosiloxane in 2-methyltetrahydrofuran (2-MeTHF) as the solvent. A wide range of aryl and alkyl α-keto amides, prepared from anilines and alkylamines, were subjected to the hydrosilylation conditions to afford α-hydroxy amides in moderate to excellent yields. This transition-metal-free protocol was applied to a chemoselective hydrosilylation, in which reduction occurred at the carbonyl of the α-keto amide functionality over that of the simple ketone, and further extended to a gram-scale protocol.

Potassium Phosphate-Catalyzed Chemoselective Reduction of α-Keto Amides: Route to Synthesize Passerini Adducts and 3-Phenyloxindoles

Muthukumar, Alagesan,Mamillapalli, N. Chary,Sekar, Govindasamy

, p. 643 - 652 (2016/02/27)

A chemoselective reduction of α-keto amides to biologically important α-hydroxy amides (mandelamides) by polymethylhydrosiloxane (PMHS) using 5 mol% potassium phosphate (K3PO4) as catalyst has been developed. This transition metal-free protocol discloses excellent chemoselectivity for the ketone reduction of α-keto amides in the presence of other reducible functionalities like ketone, nitro, halides, nitrile and amide. Also, the chemoselectively reduced α-hydroxy amide has been derivatized to isocyanide-free Passerini adducts. The N-alkyl-α-hydroxy amides have been successfully converted to 3-phenyloxindole derivatives by treatment with methanesulfonyl cholride and triethylamine.

Chemoselective Reductive Deoxygenation and Reduction of α-Keto Amides by using a Palladium Catalyst

Mamillapalli, N. Chary,Sekar, Govindasamy

, p. 3273 - 3283 (2015/11/03)

A palladium catalyst is used to synthesize 2,N-diphenylacetamides and α-hydroxy amides from readily available α-keto amides by chemoselective reductive deoxygenation and chemoselective reduction using polymethylhydrosiloxane (PMHS). This methodology has t

ANIONIC ACTIVATION BY FLUORIDE ION IN SOLID-LIQUID SYSTEMS. SYNTHESIS OF 3 (2H)-FURANONES AND 2 (5H)-FURANONES.

Sebti, S.,Foucaud, A.

, p. 1361 - 1368 (2007/10/02)

The evolution of 2-acyloxy 2-methyl 3-oxobutanamides 1 and 2-acyloxy 3-oxo 2,3-diphenylpropanamides 13 under anionic activation by cesium fluoride was studied.The fluoride ion is an efficient base for the heterocyclization of 1 into 3 (2H)-furanones and 2 (5H)-furanones, but the hydrolysis of the ester group lowered the selectivity of the reaction.However, the cleavage of 13 into the esters 14 and the cyclization of 3-benzoyloxy 3-methyl 2-butanone into bullatenone are very selective.

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