N-tert-butyl-4-isopropylsulfonyl-benzamide

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Identification

Molecular formula
C15H23NO3S
CAS Number
622958-56-7
IUPAC Name
N-tert-butyl-4-isopropylsulfonyl-benzamide
Molecular Weight
297.42g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2100g/cm3
Synonyms
N-tert-Butyl-p-(isopropylsulfonyl)benzamide
Interesting facts

Interesting Facts about N-tert-butyl-4-isopropylsulfonyl-benzamide

N-tert-butyl-4-isopropylsulfonyl-benzamide is a fascinating compound that falls within the realm of organic chemistry. Here are some engaging aspects of this compound:

  • Versatile Applications: This compound is often explored for its potential in pharmaceuticals and organic synthesis, particularly in drug development.
  • Sulfonyl Group Significance: The presence of the sulfonyl group (–SOâ‚‚) is noteworthy as it can enhance the compound's reactivity and influence its interactions with biological systems.
  • Structure and Properties: The unique combination of the tert-butyl and isopropyl groups contributes to the compound's steric hindrance, which can affect its reactivity and binding characteristics.
  • Research Potential: Chemists are interested in compounds like N-tert-butyl-4-isopropylsulfonyl-benzamide when exploring new methods for selective functionalization in organic reactions.
  • Importance in Medicinal Chemistry: Compounds that contain both a sulfonamide and an aromatic system are often studied for their biological activities, making them potential candidates for drug discovery.
  • Reaction Pathways: Due to the structure of this compound, it has been a subject of studies on various reaction pathways, such as electrophilic substitutions and nucleophilic attacks.

In summary, N-tert-butyl-4-isopropylsulfonyl-benzamide is more than just a structural entity; it embodies a variety of chemical functional properties that make it an intriguing subject for scientists and students alike. Its relevance in medicinal chemistry and organic synthesis sheds light on the profound implications of structural modifications in compound functionality.

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