CAS 33769-07-2
:1-Trityl-1H-imidazole-4-methanol
Description:
1-Trityl-1H-imidazole-4-methanol is a chemical compound characterized by its imidazole ring, which is a five-membered aromatic heterocycle containing two nitrogen atoms. The presence of the trityl group, a bulky phenyl group attached to a carbon atom, enhances the compound's stability and solubility in organic solvents. The methanol functional group introduces a hydroxymethyl substituent, which can participate in hydrogen bonding and may influence the compound's reactivity and interaction with other molecules. This compound is typically used in organic synthesis and may serve as an intermediate in the preparation of various pharmaceuticals or biologically active compounds. Its unique structure allows for potential applications in medicinal chemistry, particularly in the development of drugs targeting specific biological pathways. As with many organic compounds, its properties such as solubility, melting point, and reactivity can vary based on the solvent and conditions used in experiments. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C23H20N2O
InChI:InChI=1/C23H20N2O/c26-17-22-16-25(18-24-22)23(19-10-4-1-5-11-19,20-12-6-2-7-13-20)21-14-8-3-9-15-21/h1-16,18,26H,17H2
SMILES:c1ccc(cc1)C(c1ccccc1)(c1ccccc1)n1cc(CO)nc1
Synonyms:- (1-trityl-1H-imidazol-4-yl)methanol
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Found 5 products.
1-TRITYL-1H-IMIDAZOLE-4-METHANOL
CAS:Formula:C23H20N2OPurity:95%Color and Shape:SolidMolecular weight:340.4177(1-Trityl-1H-imidazol-4-yl)methanol
CAS:<p>(1-Trityl-1H-imidazol-4-yl)methanol</p>Purity:97%Molecular weight:340.42g/molMedetomidine Impurity 35
CAS:Formula:C23H20N2OColor and Shape:Pale Yellow SolidMolecular weight:340.431-Trityl-1h-imidazole-4-methanol
CAS:<p>1-Trityl-1H-imidazole-4-methanol is a compound that has been shown to have anti-cancer properties. It is a picolinic acid analogue and can be used for the treatment of cancer. This drug has been shown to inhibit the growth of cells in cultures from human breast carcinoma, leukemia, and lymphoma. 1-Trityl-1H-imidazole-4-methanol binds to the carboxylate moiety of proteins and inhibits protein synthesis by competitively inhibiting the binding of aminoacyl tRNA to ribosomes. The nitro group on this molecule may also contribute to its anticancer activity, as it can be reduced by cytochrome P450 enzymes in the liver into reactive species that react with DNA. This drug is water soluble and is therefore more easily excreted than other picolinic acid analogues. 1-Trityl-1H-imid</p>Formula:C23H20N2OPurity:Min. 95%Molecular weight:340.42 g/mol




