Methyl 4-aminobenzenesulfonylcarbamate
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- Molecular formula
- C8H10N2O4S
- CAS Number
- 69644-56-4
- IUPAC Name
- methyl N-(4-aminophenyl)sulfonylcarbamate
- Molecular Weight
- 230.25g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4115g/cm3
- Synonyms
- ASULAM
Identification
Interesting facts
Interesting Facts about Methyl N-(4-Aminophenyl)sulfonylcarbamate
Methyl N-(4-aminophenyl)sulfonylcarbamate is a fascinating compound with diverse applications and unique characteristics. Below are some intriguing insights about this compound:
- Biological Significance: This compound is a key player in medicinal chemistry. Its structure allows it to interact effectively with biological targets, making it a candidate for drug development.
- Mechanism of Action: Methyl N-(4-aminophenyl)sulfonylcarbamate may act through mechanisms such as inhibition or modulation of specific enzymes, contributing to its therapeutic effects.
- Sulfonamide Derivative: As a sulfonamide derivative, it inherits properties that can aid in the synthesis of similar compounds, potentially leading to novel therapeutic agents.
- Research Applications: This compound has drawn interest in the field of organic synthesis. Researchers are exploring its properties for creating more complex chemical entities.
- Environmental Considerations: Studies on its ecological impact are important, as both sulfonamide compounds and the related sulfonyl groups have been examined for their effects on the environment.
In summary, methyl N-(4-aminophenyl)sulfonylcarbamate not only showcases the elegance of organic synthesis but also holds promise in advancing medicinal research. The ongoing exploration of its properties is a testament to the vibrant and evolving field of chemistry.
"Chemistry is the life blood of every process in the universe," and compounds like methyl N-(4-aminophenyl)sulfonylcarbamate exemplify this truth in their potential to influence health and industry.