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• 2. Improving the yield of graphene oxide-catalysed N-heterocyclization of amines through fed batch mode
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• 3. Cs2CO3-promoted polycondensation of CO2 with diols and dihalides for the synthesis of miscellaneous polycarbonates
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• 4. Synthesis and properties of polyesters derived from renewable eugenol and α,ω-diols via a continuous overheating method
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• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Organobromides Organobromides
• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Organobromides
• Solvents and Organic Chemicals Organic Compounds Organic Halides
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons
• Pesticide Chemicals Pesticide Intermediates
• Pharmaceutical and Biochemical Products Pharmaceutical Intermediates

Chemical Profile of 1,4-Dibromobutane (CAS No. 110-52-1)

1,4-Dibromobutane, with the chemical formula C?H?Br?, is a significant organic compound widely utilized in synthetic chemistry and material science. This brominated alkane, identified by its CAS number 110-52-1, exhibits a unique molecular structure that makes it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty polymers. The presence of two bromine atoms at the 1st and 4th carbon positions imparts distinct reactivity, enabling diverse chemical transformations that are pivotal for modern industrial applications.

The compound’s utility stems from its ability to undergo nucleophilic substitution reactions, cross-coupling reactions, and other functional group interconversions. In pharmaceutical research, 1,4-dibromobutane serves as a precursor for the development of novel therapeutic agents. Recent studies have highlighted its role in constructing complex molecular architectures essential for drug discovery. For instance, researchers have leveraged its reactivity to synthesize brominated heterocycles, which are known to exhibit potent biological activity. These findings underscore the importance of CAS no 110-52-1 in advancing medicinal chemistry.

In material science, 1,4-dibromobutane finds application in the synthesis of flame-retardant polymers and liquid crystals. Its bromine atoms enhance the thermal stability and fire resistance of polymer matrices, making it a preferred choice for high-performance materials used in electronics and construction industries. The compound’s compatibility with various polymerization techniques has led to the development of advanced composites with tailored properties. Such innovations reflect the growing demand for 1,4-dibromobutane in industrial applications driven by sustainability and safety considerations.

From an academic perspective, 1,4-dibromobutane has been extensively studied for its mechanistic insights into organic reactions. Its role as a dibromo intermediate has provided chemists with a deeper understanding of radical-mediated transformations and stereoselective synthesis. Researchers have employed computational methods to model the reactivity of CAS no 110-52-1, revealing novel pathways for optimizing synthetic routes. These advancements not only enhance laboratory efficiency but also contribute to the broader field of organic synthesis.

The pharmaceutical industry has particularly benefited from the versatility of 1,4-dibromobutane in drug development. Its incorporation into active pharmaceutical ingredients (APIs) has enabled the creation of compounds with improved pharmacokinetic profiles. For example, derivatives of this compound have been investigated for their antimicrobial and anti-inflammatory properties. The ongoing exploration of its pharmacological potential continues to inspire new research directions, reinforcing its significance in modern medicine.

Moreover, 1,4-dibromobutane plays a crucial role in agrochemical formulations. Its derivatives are used as intermediates in the synthesis of pesticides and herbicides that enhance crop protection strategies. The compound’s ability to introduce bromine atoms into target molecules allows for the development of agrochemicals with enhanced efficacy and environmental compatibility. This aligns with global efforts to promote sustainable agriculture while maintaining high yields.

The industrial production of CAS no 110-52-1 adheres to stringent quality control measures to ensure consistency and purity. Manufacturers employ advanced purification techniques such as distillation and crystallization to isolate high-purity grades suitable for sensitive applications. These processes are critical in maintaining the compound’s reactivity and performance across various end-use industries.

In conclusion, 1,4-dibromobutane is a multifaceted compound with far-reaching applications in pharmaceuticals, materials science, and agriculture. Its unique chemical properties continue to drive innovation across multiple scientific disciplines. As research progresses, new methodologies and applications will likely emerge, further solidifying its importance in industrial and academic settings.

• 223487-53-4(1-Bromobutane-2,2,3,3,4,4,4-d7)
• 1219805-80-7(1-Bromobutane-1,1,2,2-d4)
• 55724-40-8(1-bromobutane-2,2-d2)
• 1219805-37-4(1-Bromobutane-3,3,4,4,4-d5)
• 68375-92-8(1,4-Dibromobutane-d8)
• 98195-36-9(1-Bromobutane-d9)
• 36684-45-4(1,4-Dibromobutane-1,1,4,4-d4)
• 26602-89-1(Butane, bromo-)
• 52089-63-1(1,4-Dibromobutane-2,2,3,3-d4)
• 55724-42-0(1-Bromobutane-d3)