• 2-(9,9-Di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS 302554-81-0) - TCI D5371 - AMI Scientific
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TCI

CAS 302554-81-0

2-(9,9-Di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI D5371

2-(9,9-Di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI D5371
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Rp 3.927.000,00
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This chemical compound, known as 2-(9,9-Di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, is a key organoboron reagent widely used in chemical synthesis, particularly in coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile tool in organic laboratories, enabling the formation of complex molecules through its reactive boron group. Its structural complexity and stability under controlled conditions make it an essential component in modern synthetic chemistry.

As an organoboron reagent, this compound is prized for its ability to form stable and reactive intermediates. Its non-mercurial and non-toxic nature enhances its safety profile compared to other organometallic reagents. This makes it a preferred choice for researchers seeking reliable and safe alternatives in their synthetic processes. The compound’s reactivity and stability under specific conditions further contribute to its effectiveness in various chemical applications.

In Indonesian laboratories, this reagent is commonly used in organic chemistry research, especially in academic and research institutions. Its role in facilitating the synthesis of complex organic compounds aligns with the goals of both educational and industrial research. The compound’s utility in creating new compounds with potential applications in multiple fields underscores its importance in the chemical research landscape of Indonesia.

  • Organic synthesis applications benefit from this reagent’s ability to participate in coupling reactions, enhancing the efficiency of complex molecule formation.
  • It is ideal for Suzuki-Miyaura coupling reactions due to its stability and reactivity, making it a preferred choice in cross-coupling processes.
  • In academic research settings, it supports the development of new compounds with potential applications in pharmaceuticals and materials science.
  • Its non-toxic nature makes it suitable for use in educational laboratories where safety is a priority.
  • It is commonly used in the synthesis of functionalized aromatic compounds, offering versatility in reaction pathways.

Brand TCI
CAS number 302554-81-0
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from moisture and direct sunlight

This reagent should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its stability. Due to its non-toxic nature, standard laboratory safety protocols should be followed, including proper ventilation and personal protective equipment. While it does not require special handling compared to other organometallic reagents, it is important to ensure that it is kept in a secure location to prevent accidental exposure. Proper storage ensures that the compound remains effective for its intended applications in chemical synthesis.

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