1-benzyl-4-azepanone

1-benzyl-4-azepanone - Names and Identifiers

Name	1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-ONE
Synonyms	4H-Azepin-4-one 1-Benzylazepan-4-on 1-benzyl-4-azepanone 1-Benzylazepan-4-one N-Benzylazepane-4-one hexahydro-1-(phenylMethyl)- 1-Benzylhexahydro-4-azepinone 1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-ONE 4H-Azepin-4-one,hexahydro-1-(phenylmethyl)- 4H-azepin-4-one, hexahydro-1-(phenylmethyl)-
CAS	1208-75-9
InChI	InChI=1/C13H17NO/c15-13-7-4-9-14(10-8-13)11-12-5-2-1-3-6-12/h1-3,5-6H,4,7-11H2

1-benzyl-4-azepanone - Physico-chemical Properties

Molecular Formula	C13H17NO
Molar Mass	203.28
Density	1.069
Boling Point	115-118 °C(Press: 0.01 Torr)
Flash Point	137.1°C
Vapor Presure	0.000355mmHg at 25°C
pKa	7.61±0.20(Predicted)
Storage Condition	under inert gas (nitrogen or Argon) at 2-8°C
Refractive Index	1.549

1-benzyl-4-azepanone - Introduction

1-Benzylhexahydroazepine-4-one is an organic compound often abbreviated as 1-Bn-1,4-imidazolidinedione. The following is an introduction to some of its properties, uses, methods and safety information:

Nature:
1-Benzylhexahydroazepin-4-one is a white solid, soluble in organic solvents such as dimethyl sulfoxide and dimethylformamide, but insoluble in water.

Use:
1-benzyl hexahydroazepin-4-one is commonly used as an intermediate in organic synthesis and can be used to synthesize a variety of organic compounds, such as herbicides, pesticides, antibiotics, etc. In addition, it can also be applied to the synthesis of drugs and the manufacture of dyes.

Method:
The main preparation method is obtained by the oxidation reaction of 1-benzyl hexahydroazepine. First, 1-benzylhexahydroazepinone is reacted with an appropriate amount of an oxidizing agent (such as hydrogen peroxide or benzoyl peroxide) under appropriate reaction conditions, and then the target product is obtained by crystallization or extraction.

Safety Information:
1-Benzylhexahydroazepine-4-one is relatively safe under routine operation, but the following matters still need to be paid attention:
-It may cause irritation to the eyes, skin and respiratory tract. Use chemical protective gloves, safety glasses and respiratory protective equipment.
-Avoid inhaling dust and skin contact. If there is contact, rinse immediately with plenty of water.
-Avoid contact with oxidants and strong acids during storage and handling to avoid dangerous reactions.
-Good ventilation conditions should be maintained in the working environment to prevent the accumulation of vapor.
-When using or handling should comply with the relevant safety procedures and disposal methods.

this information is for reference. please have a more detailed understanding and experimental operation before use.

Last Update：2024-04-09 21:01:54