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CAS 10513-45-8

N-tert-Butyl-5-methylisoxazolium Perchlorate TCI B0832

N-tert-Butyl-5-methylisoxazolium Perchlorate TCI B0832

Chemical Identity

CAS No.
10513-45-8
PubChem
CID 151520·SID 87563816
Formula
C8H14ClNO5
Molecular weight
239.65 g/mol
Purity
>98.0%(HPLC)(N)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-tert-butyl-5-methyl-1,2-oxazol-2-ium perchlorate
SMILES
CC1=CC=[N+](O1)C(C)(C)C.[O-]Cl(=O)(=O)=O
InChIKey
MPSXGPCFLAGJOM-UHFFFAOYSA-M
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N-tert-Butyl-5-methylisoxazolium Perchlorate is a synthetic reagent widely used in organic chemistry laboratories for its role in coupling reactions. This compound serves as an essential tool in the synthesis of complex organic molecules, particularly in reactions requiring electrophilic or nucleophilic activation. Its utility lies in its ability to facilitate the formation of new chemical bonds between organic compounds, making it a critical component in the development of heterocyclic compounds and isoxazol derivatives. In laboratory settings, it is often employed to streamline multi-step syntheses and improve reaction efficiency.

The compound’s chemical properties, including its high electrophilicity due to the presence of the perchlorate ion, make it a preferred choice for reactions that require activation under specific conditions. Its stability in controlled environments allows for consistent performance, while its reactivity ensures it can participate effectively in various synthetic pathways. These characteristics make it a reliable and efficient reagent for chemists working on advanced organic synthesis projects.

In Indonesian laboratories, N-tert-Butyl-5-methylisoxazolium Perchlorate is commonly used in academic and research institutions. It plays a vital role in the study of organic compounds, especially in the synthesis of aromatic and heterocyclic structures. Its application is widespread in both teaching and research environments, supporting the development of new chemical compounds and materials.

TCI brochures (PDF)

  • Organic synthesis for the preparation of heterocyclic compounds due to its electrophilic activation properties.
  • Coupling reactions where efficient bond formation between organic molecules is required.
  • Aromatics and isoxazol derivatives synthesis as it promotes nucleophilic or electrophilic attack.
  • Research applications in academic institutions for advanced chemical reactions and material development.
  • Teaching laboratories for demonstrating synthetic pathways and reaction mechanisms.

Brand TCI
CAS number 10513-45-8
Molecular formula —
Purity —
Category Chemistry > Synthetic Reagents > Coupling [Synthetic Reagents]
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from moisture and incompatible substances.

This compound should be stored in a cool, dry place, away from moisture and incompatible materials. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care in a well-ventilated area. Avoid contact with strong bases or reducing agents to prevent unwanted side reactions. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Storage conditions should be maintained to ensure stability and safety in laboratory environments.

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