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CAS 196207-58-6

2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-di-n-octylfluorene TCI B3582

2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-di-n-octylfluorene TCI B3582

Chemical Identity

CAS No.
196207-58-6
PubChem
CID 21982074·SID 125307371
Formula
C41H64B2O4
Molecular weight
642.6 g/mol
Purity
>98.0%(HPLC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-[9,9-dioctyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)fluoren-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)C4=C(C3(CCCCCCCC)CCCCCCCC)C=C(C=C4)B5OC(C(O5)(C)C)(C)C
InChIKey
FAHIZHKRQQNPLC-UHFFFAOYSA-N
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TCI B3582 196207-58-6, 2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-di-n-octylfluorene, is an organoboron compound widely used in organic chemistry laboratories. This reagent plays a crucial role in the synthesis of complex organic molecules, particularly in coupling reactions that form carbon-carbon bonds. Its unique structure allows for high reactivity and specificity, making it a valuable tool in modern synthetic chemistry. The compound is especially important in the development of new pharmaceuticals and advanced materials due to its ability to participate in multiple reaction pathways.

The compound's stability under controlled conditions, combined with its sensitivity to moisture and oxidation, makes it a preferred choice for specialized synthetic processes. The presence of boron atoms in its structure enhances its reactivity, while the alkyl chains provide additional functional versatility. These properties enable it to be used in a variety of synthetic strategies, including cross-coupling reactions such as Suzuki and Stille. Its chemical stability and reactivity make it a reliable reagent for precise chemical transformations in laboratory settings.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the synthesis of new compounds and drug development. It is also utilized in the study of organic materials and their applications in various scientific fields. Due to its high reactivity and structural versatility, it is a key reagent in the pursuit of innovative chemical solutions and advanced material development.

TCI brochures (PDF)

  • Organic synthesis applications benefit from this compound's ability to form carbon-carbon bonds in coupling reactions, allowing for the creation of complex molecular structures.
  • Drug development research utilizes this reagent for the synthesis of novel pharmaceutical compounds due to its reactivity and structural adaptability.
  • Material science studies leverage its unique molecular structure to develop advanced organic materials with specific functional properties.
  • Academic research in chemistry employs it for exploring new synthetic methodologies and reaction mechanisms in complex organic transformations.
  • Industrial chemical processes incorporate it in the production of specialty chemicals and polymers that require precise molecular control.

Brand TCI
CAS number 196207-58-6
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes —
Physical form —
Storage Store in a dry, cool place away from moisture and oxidizing agents

This compound should be stored in a dry, cool environment to prevent degradation due to moisture and oxidation. It is recommended to use airtight containers made of materials that do not react with the compound, such as glass or high-density polyethylene. Laboratory personnel should handle the material with care, using appropriate personal protective equipment to avoid exposure. Due to its sensitivity, it should be kept away from heat sources and incompatible substances. Regular monitoring of storage conditions is essential to maintain its chemical integrity and ensure safe handling in the laboratory.

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