4-[(4-Isothiocyanatophenyl)sulfonyl]morpholine
Names and Identifiers of 100060-98-8
CAS Number |
100060-98-8 |
|---|---|
IUPAC Name |
4-(4-isothiocyanatophenyl)sulfonylmorpholine |
InChI |
InChI=1S/C11H12N2O3S2/c14-18(15,13-5-7-16-8-6-13)11-3-1-10(2-4-11)12-9-17/h1-4H,5-8H2 |
InChIKey |
UXOOJOCKROBTEH-UHFFFAOYSA-N |
Canonical SMILES |
C1COCCN1S(=O)(=O)C2=CC=C(C=C2)N=C=S |
Physical and chemical properties of 100060-98-8
Exact Mass |
284.02900 |
|---|---|
LogP |
2.46050 |
Molecular Formula |
C11H12N2O3S2 |
Molecular Weight |
284.35500 |
PSA |
99.44000 |
Safety Information of 100060-98-8
Applications of 100060-98-8
This compound finds extensive applications in scientific research, particularly in:
- Proteomics: Used for labeling proteins and studying their interactions.
- Biochemical assays: Serves as a reagent in various assays to investigate enzyme activities and cellular responses.
- Pharmaceutical research: Explored for potential therapeutic applications due to its unique reactivity and biological properties.
Interaction Studies of 100060-98-8
Studies on the interactions of 4-[(4-Isothiocyanatophenyl)sulfonyl]morpholine reveal its capacity to react with different nucleophiles, which can lead to modifications in protein structures or functions. These interactions are crucial for understanding its role in biological systems and its potential effects on health.
Biological Activity of 100060-98-8
Research indicates that 4-[(4-Isothiocyanatophenyl)sulfonyl]morpholine exhibits significant biological activity. It interacts with various biological targets, particularly nucleophiles such as amines and thiols. This interaction may influence cellular processes, making it a valuable compound for studying biochemical pathways and potential therapeutic applications.

