Discover the exceptional versatility of ALLYL N-(2-AMINOETHYL)CARBAMATE HCL, a high-purity (95%) chemical compound with a molecular weight of 180.6326g/mol. This solid-form substance, identified by the CAS number 1049722-41-9, offers a unique blend of reactivity and stability, making it a valuable asset for a wide range of applications.
Handle with care, as this compound is classified as harmful if swallowed and may cause skin, eye, and respiratory irritation. Always wear appropriate personal protective equipment and store in a cool, well-ventilated area. Unlock the potential of this exceptional chemical in your next project, where its exceptional quality and performance will shine through.
Introducing ALLYL N-(2-AMINOETHYL)CARBAMATE HCL, a versatile and highly pure chemical compound that holds immense potential for researchers and scientists across various fields. With its unique chemical structure and exceptional purity, this compound has become a valuable asset in the realms of pharmaceutical development, agrochemical innovation, and advanced material synthesis.
At the heart of this compound lies a complex yet meticulously crafted molecular structure, identified by its CAS number 1049722-41-9. Boasting a molecular formula of C6H13ClN2O2 and a molecular weight of 180.6326 g/mol, ALLYL N-(2-AMINOETHYL)CARBAMATE HCL presents a unique combination of functional groups, including an allyl, an aminoethyl carbamate, and a hydrochloride moiety. This intricate design endows the compound with a diverse range of chemical properties, making it a versatile tool in the hands of researchers and scientists.
In the realm of pharmaceutical research, ALLYL N-(2-AMINOETHYL)CARBAMATE HCL shines as a valuable building block for the synthesis of innovative drug candidates. Its distinct chemical structure and functional groups allow for the development of targeted therapies, addressing a wide spectrum of health conditions. Researchers can leverage the compound's reactivity and selectivity to create novel pharmaceutical compounds with improved pharmacological profiles, enhanced efficacy, and reduced side effects.
The compound's potential extends beyond its use as a starting material; it can also serve as a crucial reagent in various synthetic pathways, enabling the exploration of new molecular architectures and the discovery of groundbreaking therapeutic solutions.
In the field of agrochemicals, ALLYL N-(2-AMINOETHYL)CARBAMATE HCL finds its niche as a key component in the development of advanced crop protection agents. Its unique chemical structure, with the presence of the aminoethyl carbamate moiety, contributes to the formulation of potent and selective pesticides, herbicides, and fungicides. These innovative agrochemical products can help safeguard crops, improve yields, and promote sustainable agricultural practices, all while minimizing environmental impact.
The compound's versatility allows researchers to explore new avenues in agrochemical development, unlocking the potential for more targeted and effective solutions that address the evolving challenges faced by modern agriculture.
Beyond the realms of pharmaceuticals and agrochemicals, ALLYL N-(2-AMINOETHYL)CARBAMATE HCL finds its way into the exciting world of material science. Researchers in this field leverage the compound's distinct chemical properties to engineer novel materials with enhanced performance characteristics. From improved mechanical strength and thermal stability to tailored optical or electrical properties, the integration of ALLYL N-(2-AMINOETHYL)CARBAMATE HCL into various material systems can lead to groundbreaking advancements in areas such as advanced coatings, polymers, and functional composites.
The compound's versatility and adaptability make it a valuable asset in the pursuit of innovative materials that can address the evolving needs of diverse industries, from electronics to aerospace and beyond.
ALLYL N-(2-AMINOETHYL)CARBAMATE HCL is a high-purity compound, with a reported purity of 95%. Its chemical identity is further defined by its InChI code, InChI=1S/C6H12N2O2.ClH/c1-2-5-10-6(9)8-4-3-7;/h2H,1,3-5,7H2,(H,8,9);1H, and its InChIKey, QDHZJBPUFKOFBA-UHFFFAOYSA-N, providing a unique identifier for researchers and scientists.
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