Quinoline-2-sulfonyl Fluoride
CAS No.:
878376-36-4
M. Wt:
211.21
M. Fa:
C9H6FNO2S
InChI Key:
GNNTZHUFNOYUQO-UHFFFAOYSA-N
Names and Identifiers of Quinoline-2-sulfonyl Fluoride
CAS Number |
878376-36-4 |
|---|---|
EC Number |
826-292-7 |
IUPAC Name |
quinoline-2-sulfonyl fluoride |
InChI |
InChI=1S/C9H6FNO2S/c10-14(12,13)9-6-5-7-3-1-2-4-8(7)11-9/h1-6H |
InChIKey |
GNNTZHUFNOYUQO-UHFFFAOYSA-N |
Canonical SMILES |
C1=CC=C2C(=C1)C=CC(=N2)S(=O)(=O)F |
Physical and chemical properties of Quinoline-2-sulfonyl Fluoride
Molecular Formula |
C9H6FNO2S |
|---|---|
Molecular Weight |
211.21 |
Safety Information of Quinoline-2-sulfonyl Fluoride
Applications of Quinoline-2-sulfonyl Fluoride
Quinoline-2-sulfonyl fluoride finds applications in various fields:
- Pharmaceuticals: Its derivatives are explored for drug development due to their biological activity.
- Material Science: Used in the synthesis of functional materials and polymers.
- Chemical Research: Acts as a reagent in organic synthesis for building complex molecules.
Interaction Studies of Quinoline-2-sulfonyl Fluoride
Studies involving quinoline-2-sulfonyl fluoride have focused on its interactions with various biological targets:
- Enzyme Binding Studies: Investigations into how these compounds interact with specific enzymes provide insights into their mechanism of action and potential therapeutic uses.
- Structure-Activity Relationship Studies: These studies help elucidate how structural modifications influence biological activity and reactivity.
Biological Activity of Quinoline-2-sulfonyl Fluoride
Quinoline derivatives, including quinoline-2-sulfonyl fluoride, exhibit various biological activities. They have been studied for their potential as:
- Antimicrobial Agents: Some quinoline derivatives show promise against bacterial and fungal infections.
- Anticancer Agents: Certain compounds have demonstrated inhibitory effects on histone deacetylases, which are relevant in cancer therapy.
- Enzyme Inhibitors: Quinoline derivatives can inhibit specific enzymes, contributing to their therapeutic potential.