109105-51-3
1-Benzyl-hexahydro-4H-azepin-4-amine
CAS: 109105-51-3
Molecular Formula: C13H20N2
109105-51-3 - Names and Identifiers
| Name | 1-Benzyl-hexahydro-4H-azepin-4-amine |
| Synonyms | 1-benzylazepan-4-amine 1-BENZYL-HEXAHYDRO-4H-AZEPIN-4-AMINE 1-Benzyl-hexahydro-4H-azepin-4-amine hexahydro-1-(phenylmethyl)-1H-Azepin-4-amine 1H-Azepin-4-aMine, hexahydro-1-(phenylMethyl)- |
| CAS | 109105-51-3 |
| InChI | InChI=1/C13H20N2/c14-13-7-4-9-15(10-8-13)11-12-5-2-1-3-6-12/h1-3,5-6,13H,4,7-11,14H2 |
109105-51-3 - Physico-chemical Properties
| Molecular Formula | C13H20N2 |
| Molar Mass | 204.31 |
| Density | 1.015g/cm3 |
| Boling Point | 300.1°C at 760 mmHg |
| Flash Point | 125.1°C |
| Vapor Presure | 0.00114mmHg at 25°C |
| Storage Condition | 2-8°C |
| Refractive Index | 1.548 |
109105-51-3 - Introduction
1-N-Benzyl-4-aminoazepane (N-Benzyl-4-aminopiperidine) is an organic compound with the chemical formula C14H22N2. The following is a brief description of its nature, use, preparation and safety information:
Nature:
1-N-benzyl-4-aminoazepane is a colorless to slightly yellow liquid with a special amino nitrogen heterocyclic structure. It has good solubility and stability, and is easy to store and use at room temperature.
Use:
1-N-benzyl-4-aminoazepane is an important intermediate in organic synthesis. It is widely used in the field of medicine to synthesize drugs, especially for the synthesis of antidepressants, local anesthetics and muscle relaxants.
Preparation Method:
The preparation of 1-N-benzyl-4-aminoazepane is usually completed through a series of organic synthesis reactions. The specific method may include the reaction of ammonia and tetrahydrofuran to synthesize N-benzyl-4-aminopiperidine intermediate, which is then further subjected to catalytic hydrogenation to obtain the final product.
Safety Information:
1-N-Benzyl-4-aminoazepane is less toxic and dangerous. However, as an organic compound, use should comply with the relevant safety procedures, avoid contact with skin and eyes, avoid inhalation or ingestion. In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical assistance. During operation, good ventilation conditions should be maintained to avoid flammable or harmful gases. At the same time, during storage and transportation, care should be taken to avoid contact with oxidants and fire sources to avoid accidents such as fire or explosion.
Nature:
1-N-benzyl-4-aminoazepane is a colorless to slightly yellow liquid with a special amino nitrogen heterocyclic structure. It has good solubility and stability, and is easy to store and use at room temperature.
Use:
1-N-benzyl-4-aminoazepane is an important intermediate in organic synthesis. It is widely used in the field of medicine to synthesize drugs, especially for the synthesis of antidepressants, local anesthetics and muscle relaxants.
Preparation Method:
The preparation of 1-N-benzyl-4-aminoazepane is usually completed through a series of organic synthesis reactions. The specific method may include the reaction of ammonia and tetrahydrofuran to synthesize N-benzyl-4-aminopiperidine intermediate, which is then further subjected to catalytic hydrogenation to obtain the final product.
Safety Information:
1-N-Benzyl-4-aminoazepane is less toxic and dangerous. However, as an organic compound, use should comply with the relevant safety procedures, avoid contact with skin and eyes, avoid inhalation or ingestion. In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical assistance. During operation, good ventilation conditions should be maintained to avoid flammable or harmful gases. At the same time, during storage and transportation, care should be taken to avoid contact with oxidants and fire sources to avoid accidents such as fire or explosion.
Last Update：2024-04-09 21:11:58
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