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Methyl-(4-phenyl-thiazol-2-yl)-amine hydrochloride is a chemical compound with the molecular formula C10H10N2S·HCl. It is a derivative of methyl-(4-phenyl-thiazol-2-yl)-amine, which is a heterocyclic compound containing a thiazole ring. The hydrochloride salt form is commonly used to improve the solubility and stability of the compound. This chemical is primarily used in pharmaceutical applications, particularly as an intermediate in the synthesis of various drugs and medicinal compounds. It is known for its potential role in modulating certain biological processes and has been studied for its therapeutic properties. The compound is typically synthesized through chemical reactions involving amines and thiazoles, and its hydrochloride form is obtained by treating the base with hydrochloric acid.

6142-12-7

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6142-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6142-12-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6142-12:
(6*6)+(5*1)+(4*4)+(3*2)+(2*1)+(1*2)=67
67 % 10 = 7
So 6142-12-7 is a valid CAS Registry Number.

6142-12-7Upstream product

6142-12-7Relevant academic research and scientific papers

INHIBITION OF CELL PROLIFERATION

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Page/Page column 48; 49; 61; 74, (2008/06/13)

The disclosed modulators of Rb:Raf-1 interactions are potent, selective disruptors of Rb:Raf-1 binding, with IC50 values ranging from 80 nM to 500 nM. Further, these compounds are surprisingly effective in inhibiting a wide variety of cancer cells, including osteosarcoma, epithelial lung carcinoma, non small cell lung carcinoma, three different pancreatic cancer cell lines, two different glioblastoma cell lines, metastatic breast cancer, melanoma, and prostate cancer. Moreover, the disclosed compounds effectively disrupt angiogenesis and significantly inhibited tumors in nude mice derived from human epithelial lung carcinoma tumors. Accordingly, the disclosed compounds, pharmaceutical compositions comprising the compounds, methods of inhibiting cell proliferation, methods of treating subjects with cancer, and methods of preparing the disclosed compounds are provided.

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