• 884336-44-1 2-(9,9'-Spirobi[fluoren]-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane - AMI Scientific
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TCI

CAS 884336-44-1

2-(9,9'-Spirobi[fluoren]-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI S0980

2-(9,9'-Spirobi[fluoren]-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane TCI S0980

Chemical Identity

CAS No.
884336-44-1
PubChem
CID 60135725·SID 354333217
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]-2-yl)-1,3,2-dioxaborolane
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC3=C(C=C2)C4=CC=CC=C4C35C6=CC=CC=C6C7=CC=CC=C57
InChIKey
VZMLUIPYIYNRGP-UHFFFAOYSA-N
Rp 1.961.400,00
Rp 1.961.400,00
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This chemical compound, 2-(9,9'-Spirobi[fluoren]-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, is an organoboron reagent with a complex molecular structure. It plays a crucial role in organic chemistry laboratories, particularly in catalytic reactions that require precise control over bond formation. Its unique chemical properties make it an essential component in various synthetic processes, supporting the development of advanced materials and pharmaceutical compounds. The compound is widely used in research settings where high reactivity and stability are required.

The compound's ability to form stable bonds with transition metals, such as palladium, makes it a preferred choice for synthetic chemists. Its controlled reactivity and structural stability allow for efficient and selective chemical transformations, which are vital in complex synthesis pathways. Additionally, its relatively non-toxic nature enhances its safety profile compared to other organoboron reagents, making it a reliable option for laboratory use. These properties contribute to its growing popularity in both academic and industrial research environments.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of pharmaceuticals and complex organic molecules. Its application in coupling reactions, such as the Suzuki reaction, supports the synthesis of heterocyclic compounds and other advanced chemical structures. Its availability and performance make it a valuable tool for researchers working on drug discovery and material science projects.

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Related TCI products

  • Organic synthesis in pharmaceutical research due to its role in coupling reactions and heterocyclic compound formation.
  • Development of advanced materials through controlled chemical transformations and stable bond formation.
  • Catalytic processes requiring organoboron reagents with high reactivity and selectivity in complex synthesis.
  • Research in drug discovery where efficient and specific chemical reactions are essential for compound development.
  • Synthesis of complex organic molecules in academic and industrial settings due to its structural stability and reactivity.

Brand TCI
CAS number 884336-44-1
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 compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which can affect its chemical properties. While the physical form is not specified, it is generally advisable to use appropriate safety measures when handling organoboron reagents. Laboratory personnel should ensure proper ventilation and follow standard safety protocols to minimize any potential risks. The compound’s relatively non-toxic nature still necessitates careful handling to ensure safe and effective use in research settings.

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