Cas no 1310923-60-4 (Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester)

Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester structure
1310923-60-4 structure
Product Name:Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester
CAS No:1310923-60-4
MF:C11H13NO2Br2
MW:351.034
CID:4530729
Update Time:2025-11-02

Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester Chemical and Physical Properties

Names and Identifiers

    • Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester

Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester Pricemore >>

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Additional information on Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester

Comprehensive Overview of Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester (CAS No. 1310923-60-4)

Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester (CAS No. 1310923-60-4) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research and fine chemical synthesis. This compound, often referred to by its systematic name, belongs to the class of carbamate esters, which are widely utilized as intermediates in the development of bioactive molecules. The presence of dibromophenyl and tert-butyl groups in its structure makes it a valuable building block for designing compounds with potential applications in medicinal chemistry and material science.

In recent years, the demand for high-purity chemical intermediates like Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester has surged, driven by advancements in drug discovery and agrochemical development. Researchers are particularly interested in its role as a protecting group or precursor in multi-step synthetic routes. The compound's unique structural features, including the bromine substituents, offer opportunities for further functionalization, making it a versatile tool in organic synthesis. This aligns with the growing trend of green chemistry, where efficient and selective transformations are prioritized.

The synthesis and characterization of Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester often involve advanced techniques such as nuclear magnetic resonance (NMR) spectroscopy and high-performance liquid chromatography (HPLC). These methods ensure the compound's purity and consistency, which are critical for its application in high-value research. Additionally, the compound's stability under various conditions makes it suitable for storage and transportation, addressing common concerns in the chemical supply chain.

From an industrial perspective, Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester is often discussed in the context of custom synthesis and contract manufacturing. Companies specializing in fine chemicals frequently highlight its availability in bulk quantities, catering to the needs of pharmaceutical companies and research institutions. The compound's compatibility with automated synthesis platforms further enhances its appeal, as it aligns with the industry's shift toward digitalization and process optimization.

Environmental and regulatory considerations also play a role in the discourse surrounding Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester. While the compound is not classified as hazardous, its handling and disposal must adhere to good laboratory practices (GLP) and international safety standards. This is particularly relevant given the increasing focus on sustainable chemistry and corporate social responsibility (CSR) in the chemical industry.

In summary, Carbamic acid, N-(2,5-dibromophenyl)-, 1,1-dimethylethyl ester (CAS No. 1310923-60-4) represents a critical intermediate in modern chemical research. Its applications span drug development, material science, and industrial synthesis, making it a subject of ongoing interest. As the scientific community continues to explore its potential, this compound is likely to remain a key player in the advancement of innovative chemical solutions.

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