• 1133057-98-3 [9-(Naphthalen-2-yl)-9H-carbazol-3-yl]boronic Acid (contains varying amounts of Anhydride) - AMI Scientific
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CAS 1133057-98-3

[9-(Naphthalen-2-yl)-9H-carbazol-3-yl]boronic Acid (contains varying amounts of Anhydride) TCI N1098

[9-(Naphthalen-2-yl)-9H-carbazol-3-yl]boronic Acid (contains varying amounts of Anhydride) TCI N1098

Chemical Identity

CAS No.
1133057-98-3
PubChem
CID 77231484·SID 468592467
Formula
C22H16BNO2
Molecular weight
337.2 g/mol
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(9-naphthalen-2-ylcarbazol-3-yl)boronic acid
SMILES
B(C1=CC2=C(C=C1)N(C3=CC=CC=C32)C4=CC5=CC=CC=C5C=C4)(O)O
InChIKey
NJKCFLBYPCPLOS-UHFFFAOYSA-N
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[9-(Naphthalen-2-yl)-9H-carbazol-3-yl]boronic Acid is a complex organoboron compound widely used in organic chemistry laboratories. This reagent plays a crucial role in various synthetic reactions, particularly in the construction of carbon-carbon bonds. Its unique structure makes it a valuable component in the development of heterocyclic compounds and boronic acid derivatives. Due to its reactivity and versatility, it is an essential tool for researchers working on advanced molecular synthesis.

The compound is known for its ability to react under specific conditions, making it a preferred choice in coupling reactions such as Suzuki and Kumada. Its solubility in organic solvents simplifies the preparation of reaction mixtures, while its stability under controlled conditions ensures reliable results. These properties make it a go-to reagent for laboratories requiring precision and consistency in their synthetic processes.

In Indonesian laboratories, this compound is commonly used by chemists and pharmacologists for the development of new compounds, including pharmaceuticals and industrial chemicals. Its application spans across research and development in both academic and industrial settings. The compound’s role in creating complex molecular structures is vital for advancing chemical innovation in the region.

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  • Organic synthesis reactions where carbon-carbon bond formation is required, due to its reactivity and compatibility with coupling mechanisms.
  • Development of heterocyclic compounds, as its structure allows for the formation of complex ring systems in synthetic pathways.
  • Pharmaceutical research, where it is used to synthesize boronic acid derivatives for drug development and chemical innovation.
  • Industrial chemical production, as it contributes to the creation of boron-containing compounds used in various applications.
  • Advanced molecular synthesis projects, where its unique reactivity supports the construction of complex organic molecules.

Brand TCI
CAS number 1133057-98-3
Molecular formula —
Purity —
Category Chemistry > Organometallic Reagents > Organoboron
Pack sizes —
Physical form Solid
Storage Keep 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 stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid exposure to incompatible substances, and ensure that storage conditions are consistent with standard laboratory safety protocols. Proper labeling and storage are essential to ensure safe handling and long-term usability in research settings.

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