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6110-53-8

(Z)-1-Bromooctadec-9-ene

Catalog#: AR003U6B  |   CAS#: 6110-53-8  |   MDL#: MFCD00083459  |   MF: C18H35Br  |   MW: 331.3745

Packsize Purity Price Availability Quantity
100mg 98% $77.00 Global Stock Buy Now Add To Cart
250mg 98% $130.00 Global Stock Buy Now Add To Cart
1g 98% $339.00 Global Stock Buy Now Add To Cart
5g 98% $1,084.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003U6B
Chemical Name (Z)-1-Bromooctadec-9-ene
CAS Number 6110-53-8
Molecular Formula C18H35Br
Molecular Weight 331.3745
MDL Number MFCD00083459
SMILES CCCCCCCC/C=CCCCCCCCCBr

(Z)-1-Bromooctadec-9-ene, a chemical compound with the molecular formula C18H35Br, holds significant importance in chemical synthesis processes. It serves as a versatile building block in organic chemistry, specifically known for its role as an intermediate in the synthesis of various compounds. The presence of a bromine group on the ninth carbon atom of the octadecene chain allows for strategic chemical transformations, enabling the creation of diverse molecular structures.In the realm of chemical synthesis, (Z)-1-Bromooctadec-9-ene finds applications in the preparation of lipid derivatives, which are crucial in the pharmaceutical and cosmetic industries. By utilizing this compound as a starting material, chemists can introduce specific functional groups and modify the molecular structure to tailor properties such as solubility, stability, and bioactivity. Additionally, (Z)-1-Bromooctadec-9-ene can be employed in the synthesis of surfactants, lubricants, and other specialty chemicals that play essential roles in various industrial processes.Furthermore, the selective reactivity of the bromine atom in (Z)-1-Bromooctadec-9-ene allows for regioselective and stereoselective transformations, leading to the controlled formation of complex molecules with high purity and efficiency. Its incorporation into synthetic pathways enables chemists to access diverse chemical space, facilitating the discovery and development of novel materials and compounds with tailored properties for specific applications. By harnessing the unique reactivity of (Z)-1-Bromooctadec-9-ene, researchers can unlock new possibilities in organic synthesis and expand the scope of chemical innovation.
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