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TCI

CAS 1161009-89-7

2-(9,9'-Spirobi[fluoren]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI S0994

2-(9,9'-Spirobi[fluoren]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI S0994

Chemical Identity

CAS No.
1161009-89-7
PubChem
CID 69676279·SID 354334791
Formula
C31H27BO2
Molecular weight
442.4 g/mol
Purity
>98.0%(HPLC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4,4,5,5-tetramethyl-2-(9,9'-spirobi[fluorene]-4'-yl)-1,3,2-dioxaborolane
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=C3C4=CC=CC=C4C5(C3=CC=C2)C6=CC=CC=C6C7=CC=CC=C57
InChIKey
GPTMWZAAIQOCLM-UHFFFAOYSA-N
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2-(9,9'-Spirobi[fluoren]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a specialized organoboron reagent used in advanced organic chemistry applications. This compound plays a crucial role in laboratory settings where complex molecular structures and precise chemical modifications are required. It is particularly valuable for its ability to participate in various coupling reactions, making it an essential tool for synthetic chemists. Its unique molecular structure, featuring a spirobi[fluoren] core, contributes to its reactivity and stability, allowing it to be used in a wide range of chemical transformations.

The compound’s organoboron functionality makes it a preferred choice for its reactivity and compatibility with a variety of reaction conditions. Its stability under certain synthetic conditions ensures reliable results in laboratory experiments. Additionally, its molecular design allows for selective participation in reactions, which is critical for achieving desired chemical outcomes. These properties make it a versatile reagent in both academic and industrial research environments.

In Indonesian laboratories, this compound is widely used in organic chemistry research, particularly in universities and research institutions. Its availability and effectiveness in complex synthesis make it a popular choice among chemists working on pharmaceutical and material science projects. The compound’s role in coupling reactions, such as Suzuki-Miyaura, further solidifies its importance in modern chemical synthesis.

TCI brochures (PDF)

  • Complex molecule synthesis requires a stable and reactive organoboron reagent to achieve precise structural modifications.
  • Suzuki-Miyaura coupling reactions benefit from this compound’s ability to form stable boronic acid derivatives for cross-coupling.
  • Pharmaceutical research utilizes this reagent for the synthesis of bioactive compounds with specific functional groups.
  • Organic synthesis in academic settings relies on its versatility and compatibility with various reaction conditions.
  • Material science applications use its reactivity to develop new polymers and functional materials with tailored properties.

Brand TCI
CAS number 1161009-89-7
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid or liquid, depending on the specific formulation
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 reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture, which could affect its stability. Proper ventilation is essential when handling the material to minimize inhalation risks. The container should be made of a material compatible with the compound’s chemical properties, such as glass or high-density polyethylene. Always follow standard laboratory safety protocols, including the use of personal protective equipment, to ensure safe handling and storage.

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