Aclidinium bromide

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Identification

Molecular formula
C26H38ClNO4
CAS Number
320345-99-1
IUPAC Name
2-piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate;chloride
Molecular Weight
489.88g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2479g/cm3
Appearance
without any discolorations or impurities visible to the naked eye.
Synonyms
3-Chloro-2-methylcarbanilic acid 2-piperidinoethyl ester hydrochloride
Interesting facts

Interesting Facts About 2-Piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate; Chloride

2-Piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate; chloride is an intriguing compound that showcases the versatility of chemical structures and their applications. Here are some engaging insights:

  • Pharmaceutical Relevance: This compound is often studied for its potential role in drug development and medicinal chemistry. The presence of the piperidine ring is significant as it is a common motif in many drugs, conferring favorable biological activity.
  • Quaternization Effect: The quaternization of the piperidine nitrogen gives rise to cationic species, which can enhance the compound's interaction with biological membranes and improve its absorption and distribution.
  • Chloro-Substituted Phenyl Ring: The presence of the 3-chloro-2-methyl-phenyl moiety adds chemical diversity and contributes to the compound’s reactivity profile, making it a subject of interest in synthetic organic chemistry.
  • Functionality: The carbamate functional group plays a crucial role in the compound's behavior and stability. Carbamates are known for their activity in agrochemicals and could be explored for their potential in developing insecticides or herbicides.
  • Synthetic Pathway: The synthesis of this compound may involve complex multi-step reactions, which allow chemists to explore various synthetic methodologies and reaction conditions.

According to chemists, "The beauty of compound design lies in the subtle balance of structure and function." This is particularly true for 2-piperidin-1-ium-1-ylethyl N-(3-chloro-2-methyl-phenyl)carbamate; chloride as researchers continue to unlock its potential.

In summary, this compound not only serves as a chemical curiosity but also opens doors to various applications across pharmaceuticals and agrochemicals, reflecting the dynamic interplay between structure, reactivity, and application in the field of chemistry.

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