Carbamate

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Identification

Molecular formula
C9H12N2O2
CAS Number
1646-88-4
IUPAC Name
(3-aminophenyl) N,N-dimethylcarbamate
Molecular Weight
180.20g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0280g/cm3
Synonyms
3-AMINOPHENYL DIMETHYLCARBAMATE
Interesting facts

Interesting Facts about (3-aminophenyl) N,N-dimethylcarbamate

(3-aminophenyl) N,N-dimethylcarbamate, also known in some contexts as a form of a carbamate compound, is noteworthy for several intriguing aspects:

  • Biological Relevance: This compound has gained attention in pharmacology and biochemistry due to its potential as a pharmaceutical intermediate. Its structure allows for the modification that can lead to various bioactive agents.
  • Mechanistic Insights: Compounds like (3-aminophenyl) N,N-dimethylcarbamate are often studied for their inhibitory effects on key enzymes. This can grant insights into their mechanisms of action, which is essential for drug development.
  • Environmental Impact: The carbamate class of compounds is significant in environmental chemistry, where their degradation pathways are crucial for understanding toxicity and biodegradability. This makes them relevant in studies of pollution and environmental safety.
  • Structure-Activity Relationships: Chemists are fascinated by how slight variations in the carbon chain or amino groups can lead to drastic changes in the pharmacological activity of these compounds. This relation is essential for rational drug design.

In summary, the study of (3-aminophenyl) N,N-dimethylcarbamate encompasses various scientific disciplines, offering a rich field for exploration in both medicinal chemistry and environmental science. Its dual roles underline the importance of such compounds in both therapeutic applications and ecological considerations.

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