CAS 284462-37-9
:4-(4-Aminophenoxy)-N-methylpicolinamide
Description:
4-(4-Aminophenoxy)-N-methylpicolinamide, identified by its CAS number 284462-37-9, is a chemical compound that features a picolinamide structure with an aminophenoxy group. This compound typically exhibits characteristics such as being a solid at room temperature, with potential applications in medicinal chemistry due to its structural motifs that may interact with biological targets. The presence of the amino group suggests it may participate in hydrogen bonding, enhancing its solubility in polar solvents. Additionally, the methyl group on the nitrogen atom can influence its lipophilicity and overall pharmacokinetic properties. The compound may also exhibit specific reactivity patterns typical of amides and aromatic compounds, making it of interest for further research in drug development or as a chemical probe in biological studies. Its synthesis and characterization would involve standard organic chemistry techniques, and its stability and reactivity would depend on the surrounding conditions, such as pH and temperature.
Formula:C13H13N3O2
InChI:InChI=1S/C13H13N3O2/c1-15-13(17)12-8-11(6-7-16-12)18-10-4-2-9(14)3-5-10/h2-8H,14H2,1H3,(H,15,17)
InChI key:InChIKey=RXZZBPYPZLAEFC-UHFFFAOYSA-N
SMILES:O(C=1C=C(C(NC)=O)N=CC1)C2=CC=C(N)C=C2
Synonyms:- 2-Pyridinecarboxamide, 4-(4-aminophenoxy)-N-methyl-
- 4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide
- 4-(4-Aminophenoxy)-N-methylpicolin Amide
- 4-(4-Aminophenoxy)pyridine-2-carboxylic acid methylamide
- 4-(4-aminophenoxy)-N-methylpyridine-2-carboxamide
- 4-[2-(N-Methylcarbamyl)-4-pyridyloxy]aniline
- 4-[[2-(Methylcarbamoyl)pyridin-4-yl]oxy]aniline
- 4-[[2-(N-Methylcarbamoyl)-4-pyridyl]oxy]aniline
- 4-[[2-(N-Methylcarbamoyl)pyridin-4-yl]oxy]aniline
- N-Methyl-4-(4-aminophenoxy)pyridine-2-carboxamide
- [4-(4-Aminophenoxy)(2-Pyridyl)]-N-Methylcarboxamide
- [4-(4-Aminophenoxy-2-pyridyl)]
- 4-(4-aminophenoxy)-N-methylpyridine-2-carboxamide oxalate
- 4-(4-Aminophenyloxy)-N-methyl-2-pyridininecarboxamide
- Sorafenib INT2
- 4-(4-Aminophenoxy)-N-methylpicolinamide
- 4-(4-aMiNApheNAxy)-N-MethylpicolinaMide
- [4-(4-Aminophenoxy-2-pyridyl)]-2-methylcarboxamide
- 4-(4- aMinophenoxy)-N- Methyl-2- pyridineforMaMide
- 4-(4-AMinophenoxy)-pyridine-2-carboxylic acid aMide
- Sorafenib impurity A
- 4-[[2-(N-Methylcarbamoyl)-4-pyridyl]oxy]anilin
- 4-(4-Aminophenoxy)-N-methylpicolimide
- 4-(4-AMino-phenoxy)-pyridine-2-carboxylicacidMethylaMide
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Found 9 products.
4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide
CAS:Formula:C13H13N3O2Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow to Light orange powder to crystallineMolecular weight:243.274-(4-Aminophenoxy)-N-methylpicolinamide
CAS:Formula:C13H13N3O2Purity:98%Color and Shape:SolidMolecular weight:243.2662-Pyridinecarboxamide, 4-(4-aminophenoxy)-N-methyl-
CAS:Formula:C13H13N3O2Purity:97%Color and Shape:SolidMolecular weight:243.26124-(4-Aminophenoxy)-N-methylpyridine-2-carboxamide
CAS:<p>4-(4-Aminophenoxy)-N-methylpyridine-2-carboxamide</p>Purity:98%Color and Shape:PowderMolecular weight:243.26g/mol[4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide
CAS:Controlled ProductFormula:C13H13N3O2Color and Shape:Light BrownMolecular weight:243.26[4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide-d4
CAS:Controlled Product<p>Applications [4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide-d4 is an intermediate in the synthesis of Sorafenib-d4 (S676853); a labelled version of Sorafenib (S676850), a potent RAF kinase inhibitor.<br>References Richly, H., et al.: Int. J. Clin. Pharmacol. Ther., 41, 620 (2003);Khire, U.R., et al.: Bioorg. Med. Chem. Lett., 14, 783 (2004);Wilhelm, S.M., et al.: Cancer Res., 64, 7099 (2004);Rini, B.I., et al.: Expert Opin. Pharmacother., 7, 453 (2006)<br></p>Formula:C13D4H9N3O2Color and Shape:NeatMolecular weight:247.286[4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide
CAS:<p>4-(4-Aminophenoxy)(2-pyridyl)]-N-methylcarboxamide is a chemical compound that inhibits the growth of cancer cells by binding to the active site of b-raf and blocking its activity. It has been shown in a pharmacokinetics study that 4-(4-aminophenoxy)(2-pyridyl)]-N-methylcarboxamide is absorbed rapidly through the oral administration, excreted in urine, and eliminated rapidly from the body. The optimal reaction for this drug was found to be at pH 7.0 with an ionic strength of 0.1 M (sodium chloride). This drug also has significant inhibitory activities against human cervical carcinoma and breast cancer cell lines (MDA-MB-231).</p>Formula:C13H13N3O2Purity:Min. 95%Color and Shape:Off-White To Beige To Light Brown SolidMolecular weight:243.26 g/mol







