3,4,5-Trimethoxyamphetamine (TMA-5)

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Identification

Molecular formula
C18H23NO4
CAS Number
22554-39-4
IUPAC Name
3,4,5-trimethoxy-N-(1-methyl-2-phenyl-ethyl)benzamide
Molecular Weight
297.37g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1020g/cm3
Synonyms
18341-14-5
Interesting facts

Interesting Facts about 3,4,5-trimethoxy-N-(1-methyl-2-phenyl-ethyl)benzamide

This compound, known as 3,4,5-trimethoxy-N-(1-methyl-2-phenyl-ethyl)benzamide, presents a fascinating example of how organic chemistry can lead to diverse applications and solutions. Here are some engaging insights about this unique compound:

  • Pharmacological Potential: Compounds like this one are often studied for their potential therapeutic effects, particularly in the fields of psychiatry and neurology. Researchers are interested in the compound's interaction with various receptors in the brain, which could lead to breakthroughs in treatments for mood disorders.
  • Structural Versatility: The structure of this compound includes multiple methoxy groups and a benzamide moiety, which enhances its ability to participate in various chemical reactions. This structural flexibility is crucial in the synthesis of more complex pharmaceuticals.
  • Natural Products Inspiration: Many synthetic compounds are inspired by naturally occurring substances. The inclusion of methoxy groups further emphasizes the importance of structure in biological activity, mimicking certain natural alkaloids known for their medicinal properties.
  • Research Focus: Current research often focuses on how compounds like this can serve as templates for developing new drugs. The ongoing study of its analogs helps in understanding the SAR (structure-activity relationship) which is vital for enhancing efficacy and reducing side effects.

In summary, 3,4,5-trimethoxy-N-(1-methyl-2-phenyl-ethyl)benzamide serves as a testament to the vast potential of organic compounds in medicinal chemistry. Its unique structure and properties allow it to be of interest in ongoing research and drug development.

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