The product is 8-chloro-5,10-dihydrodibenzo[b,e][1,4]diazepin-11-one with the CAS number 50892-62-1. It is factory - supplied and comes with the best price. This chemical compound belongs to the class of dibenzo[b,e][1,4]diazepinones. The presence of the chlorine atom at the 8 - position and the specific structure of the diazepinone ring system contribute to its unique chemical and physical properties.
From a physical perspective, it may have a certain melting point, boiling point, and solubility characteristics. Although specific detailed physical parameters such as melting point, boiling point, and solubility in different solvents may vary depending on the purity and synthesis conditions of the product, in general, it is important to handle it according to appropriate chemical safety procedures. It is recommended to store it in a cool, dry place away from heat sources and direct sunlight to maintain its stability.
8 - chloro - 5,10 - dihydrodibenzo[b,e][1,4]diazepin - 11 - one has a wide range of potential applications in the field of organic synthesis and pharmaceutical research. In organic synthesis, it can serve as an important intermediate for the synthesis of more complex molecules. Its unique structure can participate in various chemical reactions, such as substitution reactions, addition reactions, etc., which can be used to construct new chemical entities with specific functions.
In the pharmaceutical industry, this compound may have potential biological activities. It can be used as a lead compound for drug design and development. Scientists can modify its structure through chemical methods to optimize its biological performance, aiming to develop drugs for the treatment of various diseases such as neurological disorders, because the dibenzo[b,e][1,4]diazepine - type structure is often associated with certain interactions in the central nervous system.
When using 8 - chloro - 5,10 - dihydrodibenzo[b,e][1,4]diazepin - 11 - one, it is necessary to wear appropriate personal protective equipment, including gloves, goggles, and a lab coat. First, carefully open the container under a well - ventilated environment, such as in a fume hood, to avoid inhalation of any possible dust or vapor.
For weighing operations, use accurate weighing instruments. When using it in a chemical reaction, add it slowly to the reaction system according to the reaction protocol. The reaction conditions, such as temperature, reaction time, and the ratio of reactants, need to be strictly controlled. After the reaction is completed, appropriate post - treatment steps, such as extraction, purification, and crystallization, should be carried out to obtain the desired product.
Case 1: Organic Synthesis of a New Fluorescent Compound
In a research project focused on developing new fluorescent materials, 8 - chloro - 5,10 - dihydrodibenzo[b,e][1,4]diazepin - 11 - one was used as a key intermediate. Researchers first carried out a substitution reaction on the chlorine atom of the compound, replacing it with a functional group containing a long - chain alkane. Then, through a series of coupling reactions, they combined it with a fluorescent - active group. The final product showed excellent fluorescent properties, which could be used in biological imaging and sensor applications.
Case 2: Pharmaceutical Research for Neurological Drugs
In a pharmaceutical research team, they were exploring new drugs for treating anxiety disorders. 8 - chloro - 5,10 - dihydrodibenzo[b,e][1,4]diazepin - 11 - one was used as a starting material. By modifying its side - chain structure and introducing different substituents, they synthesized a series of derivatives. After in - vitro and in - vivo biological activity tests, some of the derivatives showed significant anxiolytic effects, which provided new leads for the development of anti - anxiety drugs.
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