
CAS 86347-12-8
:1-(2,3-DiMethylphenyl)-1-(1H-iMidazol-4-yl)ethanol
Description:
1-(2,3-Dimethylphenyl)-1-(1H-imidazol-4-yl)ethanol, with the CAS number 86347-12-8, is an organic compound characterized by its complex structure that includes a dimethyl-substituted phenyl group and an imidazole moiety. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including potential biological activity due to the presence of the imidazole ring, which is known for its role in various biochemical processes. The presence of the hydroxyl (-OH) group in the ethanol part of the molecule suggests it may engage in hydrogen bonding, influencing its solubility and reactivity. Such compounds often demonstrate interesting pharmacological properties, making them of interest in medicinal chemistry. Additionally, the steric effects introduced by the dimethyl groups can affect the compound's interaction with biological targets. Overall, this compound's unique structural features contribute to its potential applications in pharmaceuticals and other chemical industries.
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Found 7 products.
1-(2,3-Dimethylphenyl)-1-(1H-imidazol-4-yl)ethanol
CAS:Formula:C13H16N2OPurity:97%Color and Shape:SolidMolecular weight:216.2789Medetomidine Impurity 20 (Hydroxymedetomidine)
CAS:Formula:C13H16N2OColor and Shape:White To Off-White SolidMolecular weight:216.281-(2,3-Dimethylphenyl)-1-(1H-imidazol-4-yl)ethanol
CAS:<p>1-(2,3-Dimethylphenyl)-1-(1H-imidazol-4-yl)ethanol</p>Purity:97%Molecular weight:216.28g/molα-(2,3-Dimethylphenyl)-α-methyl-1H-imidazole-5-methanol
CAS:Controlled Product<p>Applications α-(2,3-Dimethylphenyl)-α-methyl-1H-imidazole-5-methanol is used as a reagent in the synthesis of Medetomidine (M203250); an α2-adrenergic agonist. Also a sedative and analgesic.<br>References Scheinin, M., et al.: Br. J. Clin. Pharmacol., 24, 443 (1987); Stenberg, D., et al.: J. Vet. Pharmacol. Ther., 10, 319 (1987); Virtanen, R., et al.: Eur. J. Pharmacol., 150, 9 (1988); Cullen, L.K., et al.: Br. Vet. J., 152, 519 (1996); Chen, W., et al.: Faming Zhuanli Shenqing. CN 101921234 A 20101222. Dec 22, 2010<br></p>Formula:C13H16N2OColor and Shape:Light Yellow To BeigeMolecular weight:216.281-(2,3-Dimethylphenyl)-1-(1H-imidazol-5-yl)ethanol
CAS:<p>1-(2,3-Dimethylphenyl)-1-(1H-imidazol-5-yl)ethanol is a versatile intermediate and building block for the synthesis of complex compounds. It is a high quality chemical that can be used as a synthetic intermediate for the production of pharmaceuticals. 1-(2,3-Dimethylphenyl)-1-(1H-imidazol-5-yl)ethanol has been shown to react with various nucleophiles to produce new scaffolds and products. This compound is also an effective reagent for use in research laboratories, such as in the study of organic reactions.</p>Formula:C13H16N2OPurity:Min. 95%Color and Shape:PowderMolecular weight:216.28 g/molα-(2,3-Dimethylphenyl)-α-methyl-1H-imidazole-5-methanol-d3
CAS:Controlled Product<p>Applications α-(2,3-Dimethylphenyl)-α-methyl-1H-imidazole-5-methanol-d3 is the isotope labelled analog of α-(2,3-Dimethylphenyl)-α-methyl-1H-imidazole-5-methanol (D473780); a reagent in the synthesis of Medetomidine (M203250) which is an α2-adrenergic agonist. Also a sedative and analgesic.<br>References Scheinin, M., et al.: Br. J. Clin. Pharmacol., 24, 443 (1987); Stenberg, D., et al.: J. Vet. Pharmacol. Ther., 10, 319 (1987); Virtanen, R., et al.: Eur. J. Pharmacol., 150, 9 (1988); Cullen, L.K., et al.: Br. Vet. J., 152, 519 (1996); Chen, W., et al.: Faming Zhuanli Shenqing. CN 101921234 A 20101222. Dec 22, 2010<br></p>Formula:C13D3H13N2OColor and Shape:NeatMolecular weight:219.297






