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Chemical Identity Revealed: CAS 36265-41-5 Explained

Apr. 18, 2024

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Chemical Identity Revealed: CAS 36265-41-5 Explained.

Welcome to our latest blog post where we delve into the intriguing world of chemical compounds. Today, we will be discussing the chemical identity of CAS 36265-41-5, a compound that has been a topic of interest among chemists and researchers.

So, what is CAS 36265-41-5? Well, CAS 36265-41-5 is the Chemical Abstracts Service (CAS) registry number for a specific compound. The CAS registry number is a unique identifier assigned to chemical substances by the American Chemical Society. This number helps researchers and scientists quickly identify and reference specific chemicals in databases and literature.

Now, let's talk about the chemical composition of CAS 36265-41-5. This compound is known by its systematic name 2-chloro-4-nitroaniline. It belongs to the class of aromatic amines, which are organic compounds containing an amine group attached to an aromatic ring. The molecular formula of 2-chloro-4-nitroaniline is C6H5ClN2O2, indicating that it contains 6 carbon atoms, 5 hydrogen atoms, 1 chlorine atom, 2 nitrogen atoms, and 2 oxygen atoms.

But what makes CAS 36265-41-5 so unique and why is it of interest to researchers? One of the reasons is its diverse range of applications. This compound is commonly used in the manufacturing of dyes and pigments, as well as in the production of agricultural chemicals. Its chemical properties make it a valuable building block in the synthesis of various organic compounds.

Another important aspect of CAS 36265-41-5 is its potential health and environmental impacts. As with any chemical compound, it is essential to understand the potential risks associated with its use and exposure. 2-chloro-4-nitroaniline has been found to be toxic to aquatic organisms and may pose risks to human health if not handled properly. Therefore, it is crucial for researchers and manufacturers to follow safety protocols and guidelines when working with this compound.

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In terms of its chemical properties, CAS 36265-41-5 exhibits interesting characteristics that make it a versatile compound. Its aromatic ring structure gives it stability and reactivity, allowing it to participate in a wide range of chemical reactions. The presence of the chloro and nitro groups in its structure also contributes to its unique properties, influencing factors such as solubility, acidity, and reactivity.

One of the key applications of 2-chloro-4-nitroaniline is in the synthesis of dyes and pigments. Its chemical structure allows it to impart vibrant colors to textile fibers and other materials. By modifying its chemical structure through various reactions, researchers can create a spectrum of different colors and shades, making it a valuable tool in the textile and dye industries.

Additionally, 2-chloro-4-nitroaniline is used in the production of agricultural chemicals such as herbicides and pesticides. Its chemical properties make it effective in targeting and controlling pests and weeds that can harm crops. By incorporating this compound into formulations, researchers can develop more potent and selective products that help protect crops and enhance agricultural productivity.

Overall, CAS 36265-41-5 is a compound that plays a significant role in various industries and research fields. Its unique chemical properties make it a valuable building block for the synthesis of organic compounds, dyes, and agricultural chemicals. However, it is crucial to understand and mitigate its potential risks to human health and the environment through proper handling and safety measures.

In conclusion, the chemical identity of CAS 36265-41-5, also known as 2-chloro-4-nitroaniline, offers a fascinating glimpse into the world of organic chemistry. Its diverse range of applications and unique chemical properties make it a compound of interest to researchers and manufacturers alike. By understanding its composition and behavior, we can harness its potential benefits while mitigating any potential risks associated with its use.

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