1-Benzyl-3-(2-bromophenyl)piperazine dihydrochloride

Unlock the versatile potential of 1-Benzyl-3-(2-bromophenyl)piperazine dihydrochloride, a meticulously crafted chemical compound that holds the key to unlocking new frontiers in scientific research and development. This highly pure and specialized molecule, identified by its CAS number 1820608-97-6, is a valuable asset for researchers and chemists seeking to explore the boundless possibilities of piperazine derivatives.

Boasting a molecular formula of C17H21BrCl2N2 and a molecular weight of 404.2 g/mol, this compound presents a unique combination of structural elements that make it a versatile tool in various scientific domains. The presence of the benzyl and 2-bromophenyl moieties, coupled with the piperazine core, endows this molecule with distinct chemical properties and reactivity, opening up a world of potential applications.

Pharmaceutical Research: Unlocking New Therapeutic Avenues

In the realm of pharmaceutical research, 1-Benzyl-3-(2-bromophenyl)piperazine dihydrochloride shines as a crucial building block in the synthesis of innovative drug candidates. Its unique structural features allow for the development of targeted therapies that address a wide range of health conditions, from neurological disorders to metabolic diseases. Researchers can leverage the compound's reactivity and selectivity to create novel pharmaceutical compounds with enhanced pharmacological profiles and improved therapeutic efficacy.

The piperazine scaffold, combined with the strategic placement of the benzyl and 2-bromophenyl groups, provides a versatile platform for the design and synthesis of diverse drug molecules. By incorporating this compound into their research workflows, pharmaceutical scientists can unlock new possibilities in the quest for more effective and safer treatments, ultimately improving patient outcomes and transforming lives.

Agrochemical Innovation: Cultivating a Greener Future

Beyond the pharmaceutical realm, 1-Benzyl-3-(2-bromophenyl)piperazine dihydrochloride also finds its place in the dynamic field of agrochemical development. Its distinct molecular structure and chemical properties contribute to the synthesis of advanced crop protection agents, helping to safeguard agricultural productivity and promote sustainable farming practices.

The strategic incorporation of this compound into agrochemical formulations can lead to the creation of potent and selective pesticides, herbicides, or fungicides. These innovative products can effectively target and eliminate pests, weeds, and plant diseases, while minimizing the environmental impact and ensuring the health and vitality of crops. By unlocking the potential of 1-Benzyl-3-(2-bromophenyl)piperazine dihydrochloride, researchers in the agrochemical industry can pave the way for a greener, more sustainable future in agriculture.

Chemical Synthesis: Unlocking Molecular Diversity

Beyond its pharmaceutical and agrochemical applications, 1-Benzyl-3-(2-bromophenyl)piperazine dihydrochloride is a valuable tool in the realm of chemical synthesis. Its unique structural features and reactivity make it a versatile building block for the creation of a wide range of novel compounds, each with their own set of tailored properties and potential applications.

Chemists and material scientists can leverage the compound's reactivity to explore new synthetic pathways, unlocking a world of molecular diversity. Whether it's the development of advanced materials, the synthesis of specialized reagents, or the exploration of unexplored chemical space, 1-Benzyl-3-(2-bromophenyl)piperazine dihydrochloride serves as a powerful catalyst for innovation and discovery.

Technical Specifications and Handling

This high-purity compound, with a minimum purity of 95%, is meticulously crafted to meet the stringent demands of scientific research and development. Its chemical identity is further defined by the MDL number MFCD28165974, providing a unique identifier for researchers seeking specific information.

To ensure the optimal performance and stability of 1-Benzyl-