• 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (CAS 408492-27-3) - TCI D5574 - AMI Scientific
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TCI

CAS 408492-27-3

2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine TCI D5574

2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine TCI D5574
Rp 2.539.950,00
Rp 2.539.950,00
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2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a specialized organic compound widely used in laboratory settings for its unique reactivity and versatility. As an organoboron reagent, it plays a crucial role in various synthetic pathways, particularly in the construction of complex molecular structures. This compound is especially valuable in the field of organic chemistry, where it serves as a key intermediate in the synthesis of heterocyclic compounds and boron-containing materials. Its ability to participate in multiple reaction types makes it a highly sought-after reagent in both academic and industrial research environments.

The compound’s reactivity is primarily attributed to its boron-containing functional group, which enables it to engage in highly selective and efficient coupling reactions. Its stability under controlled conditions further enhances its utility in laboratory applications. The presence of dichloro groups on the pyridine ring contributes to its chemical reactivity and functional versatility, making it suitable for a wide range of synthetic transformations. These properties collectively make it a preferred choice for researchers aiming to achieve high yields and precise molecular control in their experiments.

In Indonesian laboratories, this compound is commonly used in chemical research, particularly in the development of pharmaceutical compounds and industrial chemicals. Its application in Suzuki-Miyaura coupling reactions is especially prominent, where it facilitates the formation of carbon-carbon bonds with high efficiency. Researchers and students rely on this material for its reliability and performance in high-precision chemical synthesis, making it an essential component of modern laboratory workflows.

  • Suzuki-Miyaura coupling reactions for efficient carbon-carbon bond formation in heterocyclic compound synthesis.
  • Organic synthesis of pharmaceutical compounds requiring high reactivity and selectivity in boron-based reactions.
  • Development of industrial chemical intermediates through boron-mediated synthetic pathways.
  • Research in heterocyclic chemistry for the creation of complex molecular structures with functional groups.
  • Academic and industrial experimentation involving advanced organic transformation techniques.

Brand TCI
CAS number 408492-27-3
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes —
Physical form Solid
Storage Store in a cool, dry place away from moisture and light

This compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent any unwanted reactions. Due to its potential reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation is also essential when working with this material to minimize exposure. In laboratory settings, it should be stored in a designated chemical storage area that is accessible only to authorized personnel. Regular monitoring of storage conditions is advised to ensure the integrity of the compound remains unaffected.

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