CAS 312636-16-1
:4-[[4-(4-Chlorophenyl)-2-thiazolyl]amino]phenol
Description:
4-[[4-(4-Chlorophenyl)-2-thiazolyl]amino]phenol, identified by its CAS number 312636-16-1, is a chemical compound characterized by its complex structure, which includes a thiazole ring and multiple aromatic systems. This compound typically exhibits properties such as being a solid at room temperature, with potential applications in pharmaceuticals or as a research chemical due to its unique functional groups. The presence of the chlorophenyl and thiazole moieties suggests that it may possess biological activity, possibly acting as an inhibitor or modulator in various biochemical pathways. Its solubility can vary depending on the solvent, and it may exhibit specific reactivity patterns due to the amino and hydroxyl groups present in its structure. Additionally, the compound's stability, melting point, and other physical properties would be influenced by its molecular interactions and the presence of substituents. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C15H11ClN2OS
InChI:InChI=1S/C15H11ClN2OS/c16-11-3-1-10(2-4-11)14-9-20-15(18-14)17-12-5-7-13(19)8-6-12/h1-9,19H,(H,17,18)
InChI key:InChIKey=ZFGXZJKLOFCECI-UHFFFAOYSA-N
SMILES:N(C1=NC(=CS1)C2=CC=C(Cl)C=C2)C3=CC=C(O)C=C3
Synonyms:- Phenol, 4-[[4-(4-chlorophenyl)-2-thiazolyl]amino]-
- SKI 2
- SA 792728
- 4-[[4-(4-Chlorophenyl)-2-thiazolyl]amino]phenol
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Found 7 products.
4-[[4-(4-Chlorophenyl)-2-thiazolyl]amino]phenol
CAS:Formula:C15H11ClN2OSPurity:98%Color and Shape:SolidMolecular weight:302.7786SKI II
CAS:SKI II is a selective non-ATP S1P receptor inhibitor with an IC50 of 0.5 μM; it doesn't inhibit PKCα, PI3K, or ERK2.Formula:C15H11ClN2OSPurity:99.34% - 99.93%Color and Shape:SolidMolecular weight:302.784-[[4-(4-Chlorophenyl)-2-thiazolyl]amino]phenol
CAS:4-[[4-(4-Chlorophenyl)-2-thiazolyl]amino]phenol is a chemical that has been used in analytical and in vitro methods to study the cellular physiology of cells. It was found to inhibit sphingosine kinase, which is an enzyme that is involved in the synthesis of sphingosine. The inhibition of this enzyme leads to decreased levels of sphingosine and the effect on the cell. 4-[[4-(4-Chlorophenyl)-2-thiazolyl]amino]phenol can also affect mitochondrial membrane potential and cyclase activity, which may be useful for treating hyperproliferative diseases such as breast cancer.Formula:C15H11ClN2OSPurity:Min. 95%Molecular weight:302.78 g/molSKI II
CAS:Controlled Product<p>Applications SKI II is a nonlipid inhibitor of sphingosine kinase. SKI II s orally bioavailable and has shown significant inhibition of tumor growth in mice.<br>References French, K.J., et. al.: Cancer Res., 63, 5962 (2003); French, K.J., et. al.: J. Pharmacol. Exp. Ther., 318, 596 (2006)<br></p>Formula:C15H11ClN2OSColor and Shape:NeatMolecular weight:302.78






