• 9-(2-Ethylhexyl)-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole (CAS 448955-87-1) - TCI E1325 - AMI Scientific
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TCI

CAS 448955-87-1

9-(2-Ethylhexyl)-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole TCI E1325

9-(2-Ethylhexyl)-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole TCI E1325
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Rp 2.833.950,00
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9-(2-Ethylhexyl)-3,6-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is a complex organoboron compound widely used in chemical synthesis, particularly in organic chemistry. This reagent plays a crucial role in facilitating various reactions, including coupling reactions and substitution processes. Its unique molecular structure, which includes both boronic acid functionalities and a carbazole core, makes it a valuable tool for chemists working on the development of new compounds. Due to its stability and reactivity, it is often employed in advanced synthetic pathways that require precision and control.

One of the key properties that make this compound a preferred choice is its ability to participate in important reactions such as the Suzuki-Miyaura and Kumada-Corriu cross-coupling reactions. These reactions are essential in the synthesis of complex organic molecules, especially in the creation of heterocyclic structures. The presence of the boron atom allows for controlled reactivity, making it suitable for use in both academic and industrial research settings. Additionally, its stability under certain reaction conditions enhances its reliability in laboratory applications.

In Indonesian laboratories, this compound is highly relevant for researchers in organic chemistry, pharmaceutical development, and materials science. It is commonly used in studies that require precise chemical transformations and in the synthesis of compounds with specific functional groups. Its application is particularly valuable in projects that aim to develop new drugs or advanced materials, where controlled reactivity and high purity are essential.

  • Synthesis of heterocyclic compounds requiring controlled boron reactivity for efficient coupling reactions.
  • Development of pharmaceuticals where precise organic transformations are necessary for drug molecule construction.
  • Research in materials science involving the creation of complex polymers and functional materials.
  • Organic synthesis projects that demand high-purity reagents for reproducible and scalable chemical processes.
  • Advanced chemical research where stability and reactivity of organoboron compounds are critical for reaction success.

Brand TCI
CAS number 448955-87-1
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes Available in standard laboratory quantities as per supplier specifications
Physical form Solid or liquid, depending on formulation and supplier packaging
Storage —

This compound should be stored in a cool, dry, and well-ventilated area away from direct sunlight. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent contamination and maintain stability. Due to its organoboron nature, it should be handled with care, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid exposure to moisture and incompatible substances. Proper labeling and storage conditions are essential to ensure the integrity and safety of the material in the laboratory environment.

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