4-[(2-Chloro-1,3-thiazol-5-yl)sulfonyl]morpholine
Names and Identifiers of 1000925-29-0
CAS Number |
1000925-29-0 |
|---|---|
EC Number |
851-563-1 |
MDL Number |
MFCD09863302 |
IUPAC Name |
4-[(2-chloro-1,3-thiazol-5-yl)sulfonyl]morpholine |
InChI |
InChI=1S/C7H9ClN2O3S2/c8-7-9-5-6(14-7)15(11,12)10-1-3-13-4-2-10/h5H,1-4H2 |
InChIKey |
OIQRCTCSXGNYAO-UHFFFAOYSA-N |
Canonical SMILES |
C1COCCN1S(=O)(=O)C2=CN=C(S2)Cl |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000925-29-0
Boiling Point |
457.1±55.0 °C at 760 mmHg |
|---|---|
Density |
1.6±0.1 g/cm3 |
Exact Mass |
267.974304 |
Flash Point |
230.3±31.5 °C |
H Bond Acceptors |
4 |
H Bond Donors |
0 |
Index of Refraction |
1.602 |
LogP |
-0.16 |
Molecular Formula |
C7H9ClN2O3S2 |
Molecular Weight |
268.741 |
Vapour Pressure |
0.0±1.1 mmHg at 25°C |
Safety Information of 1000925-29-0
Interaction Studies of 1000925-29-0
Interaction studies involving 4-[(2-Chloro-1,3-thiazol-5-yl)sulfonyl]morpholine focus on its binding affinity to various biological targets. Preliminary studies suggest that this compound may inhibit specific enzymes or receptors implicated in disease processes. Further research is needed to elucidate these interactions fully and determine their therapeutic implications.
Biological Activity of 1000925-29-0
Research indicates that 4-[(2-Chloro-1,3-thiazol-5-yl)sulfonyl]morpholine exhibits significant biological activity, particularly in antimicrobial and antitumor domains. Its structure allows it to interact with biological targets effectively, making it a candidate for further pharmacological studies.
Antimicrobial ActivityStudies have shown that similar thiazole-based compounds possess antimicrobial properties against various bacterial strains.
Antitumor ActivityCompounds with similar structures have been evaluated for their antitumor efficacy, suggesting that 4-[(2-Chloro-1,3-thiazol-5-yl)sulfonyl]morpholine may also exhibit such properties.
