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TCI

CAS 2743539-91-3

9-(2-Biphenylyl)-10-methylacridinium Perchlorate TCI B2897

9-(2-Biphenylyl)-10-methylacridinium Perchlorate TCI B2897

Chemical Identity

CAS No.
2743539-91-3
PubChem
CID 44629816·SID 87559027
Formula
C26H20ClNO4
Molecular weight
445.9 g/mol
Purity
>98.0%(HPLC)(N)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
10-methyl-9-(2-phenylphenyl)acridin-10-ium perchlorate
SMILES
C[N+]1=C2C=CC=CC2=C(C3=CC=CC=C31)C4=CC=CC=C4C5=CC=CC=C5.[O-]Cl(=O)(=O)=O
InChIKey
BIYCHPCSVPTZJV-UHFFFAOYSA-M
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9-(2-Biphenylyl)-10-methylacridinium Perchlorate is a chemical compound widely used in catalytic and organic reactions within laboratory settings. This compound plays a crucial role in facilitating chemical transformations by acting as an organocatalyst. Its unique molecular structure enables it to participate in various reaction mechanisms, making it a valuable tool for researchers aiming to enhance reaction efficiency. The compound is particularly effective in environments where electron activation is required, allowing it to influence reaction pathways without being consumed in the process.

The compound's high reactivity and stability under specific conditions make it a preferred choice for laboratory applications. Its ability to maintain structural integrity during reactions ensures consistent performance, which is essential for reproducible results. Additionally, its compatibility with aromatic compounds enhances its utility in a range of chemical processes. The stability of this compound also contributes to its ease of storage and repeated use, making it a reliable option for long-term research projects.

In Indonesian laboratories, this compound is commonly used by chemists and researchers for various studies and development projects. Its unique properties make it a go-to material for catalytic applications, especially in substitution and oxidation reactions. The compound's effectiveness and reliability have made it a standard in both academic and industrial research settings, supporting innovation in chemical processes and product development.

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  • Catalytic Substitution Reactions: This compound is ideal for substitution reactions due to its ability to activate electron transfer, enhancing reaction efficiency in organic synthesis.
  • Oxidation Processes: Its reactivity with aromatic compounds makes it suitable for oxidation reactions, where it facilitates the conversion of substrates under controlled conditions.
  • Organic Reaction Activation: The compound's unique structure allows it to act as an efficient catalyst in organic reactions, promoting desired chemical transformations without being consumed.
  • Electronic Activation Studies: Its role in electron activation makes it valuable for research into reaction mechanisms and electronic behavior in complex chemical systems.
  • Industrial Chemical Synthesis: The compound's stability and reactivity make it a preferred choice for industrial applications requiring high-performance catalysts in large-scale chemical processes.

Brand TCI
CAS number 2743539-91-3
Molecular formula —
Purity —
Category Chemistry > Catalysis and Inorganic Chemistry > Organocatalysts [Catalysis]
Pack sizes Available in standard laboratory quantities
Physical form Solid powder
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 use airtight containers to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to heat and direct light to preserve its chemical integrity. Regular inspection of storage conditions is advised to ensure optimal performance and safety during use. Proper labeling and storage practices help maintain the compound's effectiveness and reduce the risk of accidental exposure.

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