• 1. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
• 2. Evolutionary approaches in protein engineering towards biomaterial construction
  Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
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  Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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• Solvents and Organic Chemicals Organic Compounds Alcohol/Ether

Professional Introduction to Compound with CAS No. 10160-24-4 and Product Name: 7-Bromoheptanol

7-Bromoheptanol (CAS No. 10160-24-4) is a significant compound in the field of organic chemistry and pharmaceutical research, characterized by its unique structural and functional properties. This compound, a brominated alcohol derivative, has garnered considerable attention due to its versatile applications in synthetic chemistry, drug development, and material science. The presence of a bromine substituent at the seventh carbon atom imparts distinct reactivity, making it a valuable intermediate in various chemical transformations.

The chemical structure of 7-Bromoheptanol consists of a seven-carbon chain with a hydroxyl group (-OH) at one end and a bromine atom (-Br) attached to the seventh carbon. This configuration allows for diverse functionalization possibilities, enabling its use in constructing more complex molecules. The compound’s solubility in organic solvents such as ethanol, acetone, and dichloromethane further enhances its utility in synthetic protocols.

In recent years, 7-Bromoheptanol has been extensively studied for its role in pharmaceutical synthesis. Its brominated backbone makes it an excellent precursor for the preparation of brominated heterocycles, which are prevalent in many bioactive molecules. For instance, researchers have utilized 7-Bromoheptanol to synthesize brominated pyrroles and indoles, which have shown promising biological activities as kinase inhibitors and antiviral agents. The compound’s ability to undergo nucleophilic substitution reactions facilitates the introduction of various functional groups, thereby expanding its synthetic utility.

One of the most notable applications of 7-Bromoheptanol is in the development of drug candidates targeting neurological disorders. Recent studies have highlighted its potential in the synthesis of GABA receptor modulators, which are crucial for treating conditions such as epilepsy and anxiety. The bromine atom’s electron-withdrawing effect enhances the compound’s interaction with biological targets, improving its pharmacological efficacy. Additionally, modifications of 7-Bromoheptanol have led to the discovery of novel compounds with enhanced binding affinity to specific enzymes involved in neurodegenerative diseases.

The compound’s significance extends beyond pharmaceuticals into materials science. In polymer chemistry, 7-Bromoheptanol serves as a monomer or crosslinking agent in the synthesis of specialty polymers with tailored properties. Its incorporation into polymer backbones enhances thermal stability and mechanical strength, making it valuable for high-performance materials used in aerospace and automotive industries. Furthermore, researchers have explored its use in creating conductive polymers for electronic applications, leveraging its ability to form stable radicals upon oxidation.

Advances in computational chemistry have further elucidated the reactivity patterns of 7-Bromoheptanol, providing insights into its mechanistic pathways. Molecular modeling studies have demonstrated that the compound’s bromine substituent participates in electrophilic aromatic substitution reactions more readily than other halogenated alcohols due to steric hindrance effects. This understanding has enabled chemists to design more efficient synthetic routes involving 7-Bromoheptanol, reducing reaction times and improving yields.

The environmental impact of using 7-Bromoheptanol has also been a focus of recent research. Efforts have been made to develop greener synthetic methods that minimize waste generation and hazardous byproducts. Catalytic processes utilizing transition metals have been explored as alternatives to traditional bromination techniques, offering a more sustainable approach to producing 7-Bromoheptanol on an industrial scale. Such innovations align with global efforts to promote sustainable chemistry practices.

Future directions in the study of 7-Bromoheptanol include exploring its role in medicinal chemistry beyond traditional drug development. Researchers are investigating its potential as a scaffold for designing next-generation therapeutics targeting emerging infectious diseases and cancer resistance mechanisms. The compound’s structural flexibility allows for modifications that can enhance its bioavailability and target specificity, making it an attractive candidate for personalized medicine approaches.

In conclusion,7-Bromoheptanol (CAS No. 10160-24-4) is a multifaceted compound with broad applications across multiple scientific disciplines. Its unique structural features and reactivity make it indispensable in pharmaceutical synthesis, materials science, and environmental chemistry. As research continues to uncover new possibilities for this compound,7-Bromoheptanol is poised to remain at the forefront of innovation-driven chemical applications.

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