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CAS 1219956-30-5

9-Phenyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-9H-carbazole TCI P2561

9-Phenyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-9H-carbazole TCI P2561

Chemical Identity

CAS No.
1219956-30-5
PubChem
CID 58340519·SID 354334989
Formula
C30H28BNO2
Molecular weight
445.4 g/mol
Purity
>98.0%(HPLC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
9-phenyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbazole
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)C3=CC4=C(C=C3)N(C5=CC=CC=C54)C6=CC=CC=C6
InChIKey
AIYLNDJDCBJMMY-UHFFFAOYSA-N
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9-Phenyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-9H-carbazole is a complex organoboron compound widely used in chemical laboratories for its reactivity and versatility. This compound is a key reagent in various synthetic processes, especially in the field of organic chemistry. Its unique molecular structure, featuring a boronic acid group, makes it an essential component in coupling reactions such as the Suzuki and Stille reactions. These reactions are fundamental in the synthesis of complex organic molecules, which are often used in pharmaceutical and materials science research.

The compound’s organoboron functionality provides high reactivity, particularly in reactions involving transition metal activation. Its stability under certain conditions allows for controlled chemical transformations, making it a preferred choice for precise synthetic applications. The presence of the boron group enables the formation of diverse molecular architectures, which are critical in developing new drugs and advanced materials. Its chemical stability and reactivity make it a reliable and efficient reagent for researchers aiming at high-precision synthesis.

In Indonesian laboratories, this compound is extensively used in organic chemistry research, especially in the development of pharmaceutical compounds and innovative materials. Its complex structure and reactivity make it a valuable tool for scientists working on drug discovery and material synthesis. The compound’s role in creating structurally specific molecules supports its application in both academic and industrial research settings. Its use is widespread due to its effectiveness in achieving desired chemical outcomes with high accuracy.

TCI brochures (PDF)

  • Organic synthesis applications benefit from this compound’s reactivity in coupling reactions, enabling the formation of complex molecular structures with high precision.
  • Pharmaceutical research utilizes this compound for the synthesis of drug molecules, leveraging its boronic acid functionality for efficient cross-coupling reactions.
  • Material science applications rely on its ability to form stable and functional molecular frameworks, supporting the development of advanced polymers and nanomaterials.
  • Academic research in chemistry uses it as a key reagent for exploring new synthetic pathways and understanding reaction mechanisms in organoboron chemistry.
  • Industrial chemical processes incorporate it for the production of specialty chemicals, where its reactivity and stability contribute to scalable and efficient synthesis protocols.

Brand TCI
CAS number 1219956-30-5
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid (exact form may vary depending on supplier)
Storage Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical stability. It is recommended to use airtight containers made of glass or polyethylene to prevent exposure to air and moisture. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling the compound. Proper disposal should follow standard chemical waste protocols to ensure environmental safety. The compound is not inherently hazardous under normal storage conditions but requires careful handling to maintain its effectiveness and safety in laboratory settings.

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