2-[2-(3,5-Dimethylphenoxy)ethyl]piperidinehydrochloride
2-[2-(3,5-Dimethylphenoxy)ethyl]piperidine hydrochloride
CAS: 1219961-03-1
Molecular Formula: C15H24ClNO
2-[2-(3,5-Dimethylphenoxy)ethyl]piperidinehydrochloride - Names and Identifiers
| Name | 2-[2-(3,5-Dimethylphenoxy)ethyl]piperidine hydrochloride |
| Synonyms | 2-[2-(3,5-Dimethylphenoxy)ethyl]piperidinehydrochloride 2-[2-(3,5-Dimethylphenoxy)ethyl]piperidine hydrochloride |
| CAS | 1219961-03-1 |
2-[2-(3,5-Dimethylphenoxy)ethyl]piperidinehydrochloride - Physico-chemical Properties
| Molecular Formula | C15H24ClNO |
| Molar Mass | 269.81 |
| Storage Condition | Room Temprature |
| Sensitive | IRRITANT |
| MDL | MFCD13560476 |
2-[2-(3,5-Dimethylphenoxy)ethyl]piperidinehydrochloride - Risk and Safety
| Hazard Class | IRRITANT |
2-[2-(3,5-Dimethylphenoxy)ethyl]piperidinehydrochloride - Introduction
2-[2-(3,5-Dimethylphenyl) ethyl]piperidine hydrochloride (2-[2-(3,5-dimethylphenoxy) ethyl]piperidine hydrochloride) is an organic compound. It is a powdery solid and stable at room temperature.
The compounds are commonly used as pharmaceutical intermediates and research reagents. It has analgesic and sedative effects and may be used to regulate the function of neurotransmitters. In addition, it can also be used to synthesize other organic compounds, such as anticancer drugs and pesticides.
The method for preparing this compound is to react 3,5-dimethylphenol with 2-chloroethanol to generate 2-(3,5-dimethylphenoxy) ethanol. The 2-(3,5-dimethylphenoxy) ethanol is then reacted with piperidine to produce 2-[2-(3,5-dimethylphenoxy) ethyl] piperidine. Finally, it is reacted with hydrochloric acid to give 2-[2-(3,5-dimethylphenoxy) ethyl] piperidine hydrochloride.
Regarding safety information, because the compound has certain toxicity, it is necessary to wear protective gloves and eye protection equipment during operation. Avoid inhaling dust or contact with skin. During storage and handling, care should be taken to prevent contact with oxygen, strong oxidants and strong acids to avoid dangerous reactions. In addition, the compound should be stored properly, away from fire and high temperature environment. Follow proper safety procedures and laboratory regulations. Please refer to the relevant chemical substance safety instructions during use.
The compounds are commonly used as pharmaceutical intermediates and research reagents. It has analgesic and sedative effects and may be used to regulate the function of neurotransmitters. In addition, it can also be used to synthesize other organic compounds, such as anticancer drugs and pesticides.
The method for preparing this compound is to react 3,5-dimethylphenol with 2-chloroethanol to generate 2-(3,5-dimethylphenoxy) ethanol. The 2-(3,5-dimethylphenoxy) ethanol is then reacted with piperidine to produce 2-[2-(3,5-dimethylphenoxy) ethyl] piperidine. Finally, it is reacted with hydrochloric acid to give 2-[2-(3,5-dimethylphenoxy) ethyl] piperidine hydrochloride.
Regarding safety information, because the compound has certain toxicity, it is necessary to wear protective gloves and eye protection equipment during operation. Avoid inhaling dust or contact with skin. During storage and handling, care should be taken to prevent contact with oxygen, strong oxidants and strong acids to avoid dangerous reactions. In addition, the compound should be stored properly, away from fire and high temperature environment. Follow proper safety procedures and laboratory regulations. Please refer to the relevant chemical substance safety instructions during use.
Last Update：2024-04-09 21:04:16
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