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2H-Azepin-2-one, hexahydro-1-(2-hydroxy-2-phenylethyl)- is a complex organic compound with the molecular formula C14H19NO2. It is a derivative of azepine, a seven-membered ring containing one nitrogen atom, and is characterized by its hexahydro structure, which means it has six hydrogen atoms attached to the carbon atoms in the ring. The compound features a 2-hydroxy-2-phenylethyl substituent attached to the nitrogen atom, which introduces a hydroxyl group and a phenyl group to the molecule. This specific arrangement of functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

4641-56-9

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4641-56-9 Usage

General Description

2H-Azepin-2-one, hexahydro-1-(2-hydroxy-2-phenylethyl)- is a chemical compound with a molecular formula C15H23NO2. It is commonly known by the name "N-hydroxy-2-phenylethyl-2-azepinone" and is used in the synthesis of pharmaceutical compounds and as a reagent in organic chemistry. 2H-Azepin-2-one, hexahydro-1-(2-hydroxy-2-phenylethyl)- is a white solid with a melting point of around 96-98°C and is soluble in most organic solvents. It is known for its potential medicinal properties and is a subject of ongoing research for its use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4641-56-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4641-56:
(6*4)+(5*6)+(4*4)+(3*1)+(2*5)+(1*6)=89
89 % 10 = 9
So 4641-56-9 is a valid CAS Registry Number.

4641-56-9Relevant academic research and scientific papers

Neighbour Group Participation with Reductions and Hydride Abstractions

Moehre, H.,Kamper, Ch.

, p. 512 - 520 (2007/10/02)

The reduction of N-(2-hydroxyalkyl)lactams with diisobutylaluminium hydride and the hydride ion abstraction of the corresponding amino alcohols give under neighbour group participation the fused oxazolidines.

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