1-(2,6-Difluorophenyl)cyclobutanemethanamine Hydrochloride - Names and Identifiers
1-(2,6-Difluorophenyl)cyclobutanemethanamine Hydrochloride - Physico-chemical Properties
1-(2,6-Difluorophenyl)cyclobutanemethanamine Hydrochloride - Introduction
1-(2,6-difluorophenyl) cycloputanemethanamine Hydrochloride is an organic compound with the chemical formula C11H14ClF2N. The following is a detailed description of its nature, use, preparation and safety information:
Nature:
1-(2,6-difluorophenyl) cycloputanemethanamine Hydrochloride is a solid substance, usually in the form of a white crystalline powder. It has a high melting point and boiling point, soluble in some organic solvents such as chloroform and dimethyl sulfoxide. It is stable in air, but will undergo oxidation reaction under light.
Use:
1-(2,6-difluorophenyl) cycloputanemethanamine Hydrochloride has certain applications in the field of medicine. It can be used as a pharmaceutical intermediate for the synthesis of some organic compounds with biological activity.
Method:
The preparation method of 1-(2,6-difluorophenyl) cycloputanemethanamine Hydrochloride is usually completed by synthetic chemical reactions. A common method is the reaction of 2,6-difluorobenzoic acid with cyclobutane methylamine, followed by reaction of hydrochloric acid with the intermediate product to give the desired product.
Safety Information:
The specific toxicity and risk of 1-(2,6-difluorophenyl) cycloputanemethanamine Hydrochloride is uncertain. When handling this compound, good laboratory practice should be followed and appropriate personal protective equipment such as gloves and protective glasses should be worn. Also, avoid inhaling dust and avoid contact with skin and eyes. In case of inadvertent contact, rinse with plenty of water and seek medical attention.
Please note that the above information is for reference only. For specific chemical properties and safety information, it is best to refer to the relevant chemical literature or consult a professional.
Last Update：2024-04-09 21:11:58