3-Bromo-8-methylquinolin-6-amine

Unlock the versatile potential of 3-Bromo-8-methylquinolin-6-amine, a remarkable chemical compound that holds the key to unlocking new frontiers in scientific research and development. This synthetic intermediate, identified by the CAS number 858467-31-9, boasts a unique molecular structure that makes it a valuable asset in a wide range of applications, from pharmaceutical development to agrochemical innovation.

At the heart of this compound lies a quinoline backbone, adorned with a bromine substituent at the 3-position and a methyl group at the 8-position. This strategic arrangement of functional groups endows 3-Bromo-8-methylquinolin-6-amine with exceptional properties, making it a sought-after tool for researchers and scientists across various disciplines.

Fungicidal Prowess

One of the standout features of 3-Bromo-8-methylquinolin-6-amine is its potent fungicidal activity. Studies have shown that this compound effectively inhibits the polymerization of tubulin, a critical component in the cellular structure of phytopathogens. By binding to the α subunit of tubulin, 3-Bromo-8-methylquinolin-6-amine disrupts the normal functioning of these harmful fungi, rendering them unable to proliferate and infect plants.

This remarkable fungicidal property positions 3-Bromo-8-methylquinolin-6-amine as a valuable asset in the development of advanced crop protection agents. Researchers in the agrochemical industry can leverage this compound's unique mode of action to create innovative pesticides that safeguard crops, ensuring higher yields and healthier food production.

Pharmaceutical Potential

Beyond its agrochemical applications, 3-Bromo-8-methylquinolin-6-amine also holds immense promise in the realm of pharmaceutical research and development. Its quinoline scaffold, a well-established structural motif in many drug candidates, makes it an attractive starting point for the synthesis of novel therapeutic compounds.

Researchers in the pharmaceutical industry can harness the versatility of 3-Bromo-8-methylquinolin-6-amine to explore the development of innovative drugs targeting a wide range of health conditions. The compound's ability to disrupt tubulin polymerization, for instance, could be exploited in the design of anti-cancer therapies or treatments for other diseases characterized by uncontrolled cell growth.

Synthetic Versatility

In addition to its direct applications, 3-Bromo-8-methylquinolin-6-amine serves as a valuable synthetic intermediate, enabling the creation of a diverse array of other compounds. Its bromine and methyl substituents provide reactive sites for further chemical transformations, allowing researchers to tailor the molecule's properties and functionalities to suit their specific needs.

Whether you're exploring new pharmaceutical leads, developing advanced agrochemicals, or seeking to synthesize novel materials, 3-Bromo-8-methylquinolin-6-amine stands as a versatile and powerful tool in your scientific arsenal. Its unique combination of chemical properties and potential applications makes it an indispensable asset in the pursuit of groundbreaking discoveries and innovations.

Product Specifications

• CAS Number: 858467-31-9
• Name: 3-Bromo-8-methylquinolin-6-amine
• Reference Number: 3D-IJB46731
• Description: 3-Bromo-8-methylquinolin-6-amine is a fungicidal agent that inhibits the polymerization of tubulin by binding to the α subunit of tubulin. It has been shown to be active against phytopathogens in experimental studies. 3-Bromo-8-methylquinolin-6-amine is a synthetic intermediate that can be used as a reagent for