Carisoprodol

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Identification

Molecular formula
C12H24N2O4S
CAS Number
78-44-4
IUPAC Name
ethyl N-[2-(4-hydroxy-4-phenyl-1-piperidyl)-1-methyl-ethyl]-N-phenyl-carbamate;sulfamic acid
Molecular Weight
260.34g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0845g/cm3
Synonyms
57-49-8
Interesting facts

Interesting Facts about Ethyl N-[2-(4-Hydroxy-4-Phenyl-1-Piperidyl)-1-Methyl-Ethyl]-N-Phenyl-Carbamate;

With a Touch of Sulfamic Acid

Ethyl N-[2-(4-hydroxy-4-phenyl-1-piperidyl)-1-methyl-ethyl]-N-phenyl-carbamate combined with sulfamic acid creates a fascinating intersection of medicinal chemistry and synthetic methodologies. Here are some compelling insights about this remarkable compound:

  • Pharmaceutical Relevance: This compound is a part of a broader class known as piperidine derivatives, which have gained attention due to their significance in drug design and development.
  • Mechanism of Action: Compounds like this one can act on various neurochemical pathways, potentially impacting neurotransmitters in the central nervous system and making it a candidate for treatments in various neurological disorders.
  • Sulfamic Acid Synergy: The incorporation of sulfamic acid, which is known for its versatility in organic synthesis, introduces *sulfonamide functionality*, enhancing the compound's reactivity and biological profile.
  • Versatile Applications: Beyond medicinal use, such compounds are also investigated for their roles in agricultural chemistry, particularly as protectants in plant growth systems.
  • Cyclic Structures: The piperidine ring in its structure plays a crucial role in determining both the physiochemical properties and the biological activity of the compound, showing how minor changes can result in drastic variations in effect.

As a chemistry student or a scientist, understanding the properties and interactions of such compounds opens up a wealth of opportunities in both research and industrial applications. The exploration of piperidine derivatives reinforces the mantra that *the synthesis of diverse structures can lead to discoveries that transform lives*.

In conclusion, the study of ethyl N-[2-(4-hydroxy-4-phenyl-1-piperidyl)-1-methyl-ethyl]-N-phenyl-carbamate with sulfamic acid stands as a testament to the innovation within the field of chemistry, where each compound is a key to unlocking new therapeutic avenues.

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