• 9-(2-Ethylhexyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole (CAS 856422-41-8) - TCI E1323 - AMI Scientific
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TCI

CAS 856422-41-8

9-(2-Ethylhexyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole TCI E1323

9-(2-Ethylhexyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole TCI E1323
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Rp 2.008.650,00
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9-(2-Ethylhexyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole is an organoboron compound widely used in chemical research, particularly in the synthesis of complex organic and heterocyclic molecules. This reagent plays a crucial role in modern laboratory settings by enabling precise and efficient chemical transformations. Its unique structure, combining a carbazole core with a boronic acid group, makes it highly versatile for various synthetic applications. Due to its reactivity and specificity, it is a valuable tool for chemists working on advanced organic synthesis projects.

This compound is preferred for its ability to participate in important coupling reactions, such as the Suzuki-Miyaura reaction, which is essential for constructing carbon-carbon bonds under mild conditions. The boronic acid functionality allows for selective and efficient reactions with a variety of transition metal catalysts. Additionally, its stability under controlled conditions ensures reliable performance in laboratory experiments. These properties make it a favored choice among researchers seeking to develop new compounds and materials.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in academic and industrial settings where complex molecule synthesis is required. Its application spans from basic research to the development of pharmaceuticals and advanced materials. The compound's reactivity and structural versatility make it an essential component in many chemical processes, supporting innovation and discovery in the field of chemistry.

  • Organic synthesis of heterocyclic compounds due to its reactivity in coupling reactions.
  • Development of pharmaceuticals through efficient carbon-carbon bond formation in drug molecule synthesis.
  • Advanced material research for creating novel polymers and functional compounds.
  • Catalytic processes requiring stable and reactive boronic acid groups for selective reactions.
  • Structural modification of complex molecules in academic and industrial chemical research.

Brand TCI
CAS number 856422-41-8
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 supplier packaging
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled in a well-ventilated area, ideally under a fume hood, to minimize exposure. Proper personal protective equipment, including gloves and safety goggles, should be worn during handling. The compound requires careful storage to ensure its effectiveness and safety in laboratory applications. Always follow standard chemical safety protocols to prevent accidental exposure or reaction.

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