2-Amino-5-bromo-4-t-butylthiazole

In the captivating world of organic chemistry, 2-Amino-5-bromo-4-t-butylthiazole stands out as a versatile and intriguing compound. This heterocyclic amine, identified by the CAS number 82202-32-2, is a valuable precursor in the synthesis of a wide range of compounds, each with the potential to unlock new frontiers in scientific research and innovation.

Crafted with meticulous precision, 2-Amino-5-bromo-4-t-butylthiazole boasts a unique molecular structure that sets it apart. Its core thiazole ring, adorned with a bromine substituent and a bulky t-butyl group, endows the compound with distinct chemical properties and reactivity. This intricate interplay of elements creates a canvas upon which chemists and researchers can paint their most ambitious creations.
The synthesis of 2-Amino-5-bromo-4-t-butylthiazole is a captivating tale in itself. Derived from the reaction of 1,2,3,4,5,6,7,8,9,10 erythrobenzothiadiazole with aniline and sulfuric acid, the compound's formation is marked by a fascinating kinetic isotope effect. The presence of light further accelerates the reaction, leading to the generation of a reactive intermediate that subsequently reacts with trichloroacetamide to yield the final product.

Unlocking the Potential

The versatility of 2-Amino-5-bromo-4-t-butylthiazole lies in its ability to serve as a versatile building block in a multitude of applications. In the realm of pharmaceutical research, this compound can be employed as a crucial starting material or intermediate in the synthesis of innovative drug candidates. Its unique structural features and reactivity patterns can be leveraged to develop novel therapeutics targeting a wide range of health conditions.

Beyond the pharmaceutical domain, 2-Amino-5-bromo-4-t-butylthiazole finds its way into the realm of agrochemicals. Its potential as a precursor in the synthesis of advanced crop protection agents is a testament to the compound's adaptability. The introduction of the bromine and t-butyl substituents can contribute to the development of more potent and selective pesticides, ultimately leading to healthier crops and higher yields.

The applications of 2-Amino-5-bromo-4-t-butylthiazole extend even further, as it serves as a valuable tool in the hands of chemists and material scientists. Its versatile reactivity allows for the creation of novel compounds and materials with tailored properties, opening up new avenues for scientific exploration and technological advancements.

Technical Specifications

• CAS Number: 82202-32-2
• Name: 2-Amino-5-bromo-4-t-butylthiazole
• Reference Number: 3D-HDA20232
• Molecular Formula: C7H11BrN2S
• Molecular Weight: 235.15 g/mol
• Purity: Minimum 95%
• MDL Number: MFCD03695812

Handling and Storage

As with any specialized chemical compound, proper handling and storage procedures are crucial to maintain the integrity and purity of 2-Amino-5-bromo-4-t-butylthiazole. It is recommended to store the compound in a cool, dry, and well-ventilated environment, protected from light and moisture. Adherence to standard laboratory safety protocols, including the use of personal protective equipment, is essential when working with this substance.

Unlocking the Possibilities