The Chemistry of 10-Bromodecanol (CAS 53463-68-6): Synthesis and Reactive Potential
Understanding the chemical properties and synthesis of key intermediates is fundamental to advancements in various industries. 10-Bromodecanol, with CAS number 53463-68-6, is a prime example of such a compound. This light yellow liquid, represented by the molecular formula C10H21BrO, is a crucial organic synthesis building block. Its structure, featuring a hydroxyl group at one end of a ten-carbon chain and a bromine atom at the other, imbues it with significant reactive potential, making it a sought-after specialty chemical raw material.
The synthesis of 10-Bromodecanol typically involves reactions that carefully introduce the bromine atom onto a decanol chain, or transformations from related diols or dibromoalkanes. These processes are optimized to yield high-purity material, essential for its demanding applications. When manufacturers choose to buy 10-bromodecanol online, they are seeking a reliable source that guarantees these critical CAS 53463-68-6 chemical properties. NINGBO INNO PHARMCHEM CO.,LTD. stands as a premier supplier, ensuring the consistent quality required for complex reactions.
The reactive potential of 10-Bromodecanol is extensively utilized in areas like pharmaceutical intermediate synthesis and agrochemical development. Its ability to undergo nucleophilic substitution reactions at the bromine-bearing carbon, or further functionalization at the hydroxyl group, makes it an exceptionally versatile intermediate. NINGBO INNO PHARMCHEM CO.,LTD. supports these advancements by providing this vital organic synthesis building block, facilitating the creation of sophisticated molecules that drive innovation in chemical sciences.
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Future Origin 2025
“stands as a premier supplier, ensuring the consistent quality required for complex reactions.”
Core Analyst 01
“The reactive potential of 10-Bromodecanol is extensively utilized in areas like pharmaceutical intermediate synthesis and agrochemical development.”
Silicon Seeker One
“Its ability to undergo nucleophilic substitution reactions at the bromine-bearing carbon, or further functionalization at the hydroxyl group, makes it an exceptionally versatile intermediate.”