Introduction

Chemical Property:

It is a colorless liquid with a special amino group and a cyclic structure. There are various methods for preparing (R)-3-amino tetrahydrofuran. A commonly used method is to use an enantioselective enzyme as a catalyst to perform enzyme-catalyzed resolution, separating (R)-3-amino tetrahydrofuran from a mixture. It can also be obtained through chemical methods, such as carrying out a reduction reaction in the presence of cycloheptanone to obtain the target product. It is an irritant compound, and contact with the skin or eyes may cause irritation. Additionally, it has certain toxicity to the environment and should not pollute it. During use, appropriate personal protective measures should be taken, such as wearing safety goggles, gloves, and a laboratory coat. It should be stored in a dry, well-ventilated place, away from fire and oxidizing agents.