N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-benzenesulfonamide
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- Molecular formula
- C14H21ClN2O3S
- CAS Number
- 85118-45-4
- IUPAC Name
- N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-benzenesulfonamide
- Molecular Weight
- 344.82g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3000g/cm3
- Synonyms
- TOSYLLYSINE CHLOROMETHYL KETONE
Identification
Interesting facts
Interesting Facts about N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-benzenesulfonamide
N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-benzenesulfonamide, often referred to in scientific contexts as a sulfonamide derivative, is a compound with notable pharmaceutical relevance. Here are some engaging facts about this interesting molecule:
- Pharmaceutical Applications: This compound has potential applications in drug development, particularly as an antibacterial agent due to the sulfonamide functional group, which has a long-standing history in medicinal chemistry.
- Significance of the Chloroacetyl Group: The presence of the chloroacetyl moiety enhances the reactivity of the compound, enabling various chemical transformations that can lead to the synthesis of more complex analogs.
- Role in the Body: As a sulfanilamide derivative, it may influence metabolic pathways through its interactions with enzymes. Disruption of these pathways can have therapeutic benefits.
- Structure-Activity Relationship (SAR): Investigating the SAR of this compound can yield insights into how modifications to its structure can affect antibacterial efficacy, selectivity, and pharmacokinetics.
- Importance of Amino Substitution: The amino group plays a critical role in its biological activity, making this compound of interest in the design of targeted therapies.
In essence, N-[5-amino-1-(2-chloroacetyl)pentyl]-4-methyl-benzenesulfonamide embodies the complexities of medicinal chemistry and the ongoing quest for novel therapeutic agents. As scholars and researchers delve deeper into its properties, this compound may pave the way for new discoveries in the field of pharmacology.