Discover the exceptional 2-Chloro-7-nitro-quinazolin-4-amine, a versatile Building Block with a unique molecular structure and a CAS number of 1107694-81-4. This high-quality compound boasts a molecular weight of 224.60g/mol, offering a powerful tool for your chemical research and synthesis endeavors. Crafted with precision, it presents a clear path to unlocking new possibilities in the realm of Quinazoline chemistry. Harness its exceptional properties and unlock the potential for groundbreaking discoveries, all while ensuring the safety of your laboratory environment. Elevate your experiments to new heights with this premium-grade chemical marvel.
Unlock the versatile potential of 2-Chloro-7-nitro-quinazolin-4-amine, a meticulously crafted chemical compound that holds the key to unlocking new frontiers in scientific research and development. With its unique molecular structure and exceptional purity, this Quinazoline derivative is poised to become an indispensable tool in the hands of researchers and innovators across various industries.
At the heart of this compound lies a captivating blend of chloro, nitro, and amine functional groups, each contributing to its distinct chemical profile. With a CAS number of 1107694-81-4 and a molecular weight of 224.60g/mol, 2-Chloro-7-nitro-quinazolin-4-amine is a highly specialized building block that offers a world of possibilities for those seeking to push the boundaries of scientific discovery.
In the realm of pharmaceutical research, 2-Chloro-7-nitro-quinazolin-4-amine shines as a versatile and invaluable asset. Its unique structure serves as a crucial starting material in the synthesis of innovative drug candidates, enabling researchers to explore new therapeutic avenues and address a wide range of health conditions. The compound's inherent reactivity and selectivity make it a powerful tool in the hands of medicinal chemists, unlocking the potential for groundbreaking advancements in the pharmaceutical industry.
Beyond the pharmaceutical realm, 2-Chloro-7-nitro-quinazolin-4-amine also finds its niche in the world of agrochemicals. Its distinct molecular composition contributes to the development of advanced crop protection agents, helping to safeguard agricultural yields and promote sustainable farming practices. Researchers in this field leverage the compound's unique properties to formulate potent and selective pesticides, herbicides, and other agrochemical products that address the evolving needs of modern agriculture.
In the broader realm of chemical synthesis, 2-Chloro-7-nitro-quinazolin-4-amine emerges as a versatile and indispensable tool. Its reactivity and selectivity make it a valuable reagent in the creation of novel compounds with tailored properties, opening up new avenues for material science, organic chemistry, and beyond. Researchers and chemists can harness the compound's unique characteristics to unlock groundbreaking discoveries and push the boundaries of what is possible in the world of chemical innovation.
To ensure the optimal performance and longevity of 2-Chloro-7-nitro-quinazolin-4-amine, it is essential to handle and store the compound with the utmost care. The specific hazard information is yet to be confirmed (TBC), but it is recommended to follow standard laboratory safety protocols when working with this chemical. Store the compound in a cool, dry, and well-ventilated area to maintain its stability and purity over the long term.
Embrace the transformative power of 2-Chloro-7-nitro-quinaz