• 2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine (CAS 1219956-23-6) - TCI D5271 - AMI Scientific
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TCI

CAS 1219956-23-6

2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine TCI D5271

2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine TCI D5271
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Rp 3.482.850,00
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2,4-Diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine is a complex chemical compound widely used in organometallic reactions, particularly in the synthesis of boron-containing compounds. This reagent plays a crucial role in modern organic chemistry, supporting advanced synthetic pathways that require precise molecular manipulation. Its unique structure enables it to participate in key reactions that are fundamental to the development of new materials and pharmaceuticals.

The compound is prized for its stable and reactive boron group, which allows for efficient chemical transformations under controlled laboratory conditions. Its molecular structure provides both stability and reactivity, making it suitable for a variety of synthetic applications. The non-toxic nature of the compound further enhances its appeal, as it can be safely handled in laboratory environments without significant health or safety risks.

In Indonesian laboratories, this compound is extensively used in organic chemistry research, especially in the synthesis of heteroaromatic compounds and molecular modifications. It is a key component in the development of complex organic structures, supporting both academic and industrial research efforts. Its reliability and effectiveness make it a preferred choice for researchers working on advanced chemical synthesis projects.

  • Synthetic chemistry research for the development of heteroaromatic compounds due to its reactivity and stability in boron-based reactions.
  • Organic synthesis applications in molecular modification processes, where precise chemical transformations are required.
  • Suzuki-Miyaura coupling reactions, as it serves as an efficient boron-based coupling reagent for aromatic compound synthesis.
  • Kumada-Corriu cross-coupling reactions, where its boron functionality enables the formation of complex organic structures.
  • Advanced material development projects involving the synthesis of boron-containing compounds for industrial and academic applications.

Brand TCI
CAS number 1219956-23-6
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 powder, depending on manufacturer
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical integrity and stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its reactivity. While it is considered non-toxic, standard laboratory safety protocols should still be followed, including the use of personal protective equipment when handling. The compound is stable under normal laboratory conditions and does not require special refrigeration. It is important to ensure that the storage area is well-ventilated and free from incompatible materials to prevent any potential chemical interactions.

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