
CAS 62-22-6
:1,2-Benzenediol, 4-[2-(dimethylamino)-1-hydroxyethyl]-, hydrochloride (1:1)
Description:
1,2-Benzenediol, 4-[2-(dimethylamino)-1-hydroxyethyl]-, hydrochloride (1:1), commonly known as a derivative of phenolic compounds, exhibits characteristics typical of both aromatic and amine functionalities. This compound features a benzene ring substituted with hydroxyl groups and a dimethylaminoethyl side chain, which contributes to its solubility in polar solvents. The hydrochloride form indicates that it is a salt, enhancing its stability and solubility in aqueous solutions. This compound is often studied for its potential biological activities, including antioxidant properties and effects on neurotransmitter systems, due to the presence of the dimethylamino group. Its molecular structure allows for various interactions, making it of interest in medicinal chemistry and pharmacology. Additionally, the presence of hydroxyl groups can facilitate hydrogen bonding, influencing its reactivity and interaction with other molecules. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken during use.
Formula:C10H15NO3·ClH
InChI:InChI=1S/C10H15NO3.ClH/c1-11(2)6-10(14)7-3-4-8(12)9(13)5-7;/h3-5,10,12-14H,6H2,1-2H3;1H
InChI key:InChIKey=ONSKRXJOMDVYGQ-UHFFFAOYSA-N
SMILES:C(CN(C)C)(O)C1=CC(O)=C(O)C=C1.Cl
Synonyms:- dl-N-Methylepinephrine hydrochloride
- 1,2-Benzenediol, 4-[2-(dimethylamino)-1-hydroxyethyl]-, hydrochloride, (±)-
- 1,2-Benzenediol, 4-[2-(dimethylamino)-1-hydroxyethyl]-, hydrochloride
- Benzyl alcohol, α-[(dimethylamino)methyl]-3,4-dihydroxy-, hydrochloride, (±)-
- 1,2-Benzenediol, 4-[2-(dimethylamino)-1-hydroxyethyl]-, hydrochloride (1:1)
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Found 5 products.
rac-N-Methyl Epinephrine HCl
CAS:Formula:C10H15NO3·HClColor and Shape:Off-White Semi-SolidMolecular weight:197.24 36.46rac N-Methyl Epinephrine Hydrochloride Salt
CAS:Controlled Product<p>Applications N-Methylepinephrine Hydrochloride Salt is the N-methylated analogue of the sympathomimetic hormone Epinephrine (E588585). Recent studies suggest that N-Methylepinephrine may be synthesized from Epinephrine by phenylethanolamine N-methyltransferase present in the brain.<br>References Kajita, M. et al.: Nip. Iyo Masu Sup. Gak. Kon., 19, 107 (1994); Plummer, C.J. et al.: Eur. J. Med. Chem., 148, 481 (1988);<br></p>Formula:C10H15NO3·HClColor and Shape:Off-WhiteMolecular weight:233.692rac N-Methyl Epinephrine-d6 Hydrochloride (>90%)
CAS:Controlled Product<p>Applications Labelled N-Methylepinephrine, the N-methylated analogue of the sympathomimetic hormone Epinephrine (E588585). Recent studies suggest that N-Methylepinephrine may be synthesized from Epinephrine by phenylethanolamine N-methyltransferase present in the brain.<br>References Kajita, M. et al.: Nip. Iyo Masu Sup. Gak. Kon., 19, 107 (1994); Plummer, C.J. et al.: Eur. J. Med. Chem., 148, 481 (1988);<br></p>Formula:C10H9D6NO3•HClPurity:>90%Color and Shape:Off-White To Light GreenMolecular weight:203.273646rac N-Methyl epinephrine hydrochloride salt
CAS:<p>Rac N-Methyl epinephrine hydrochloride salt is a potential anti-cancer agent that has been used in Chinese medicine for its apoptotic effects on cancer cells. It works by inhibiting the chitin kinase pathway, which is involved in tumor growth and survival. Rac N-Methyl epinephrine hydrochloride salt also acts as a potassium channel inhibitor, leading to cell death in cancer cells. This drug has shown synergistic effects when combined with other cancer treatments such as enoxaparin or heparin. Additionally, it has been found to be an effective inhibitor of psyllium-induced colon carcinogenesis in human subjects. Overall, Rac N-Methyl epinephrine hydrochloride salt shows great promise as a potential anti-cancer analog for use in cancer treatment.</p>Formula:C10H16ClNO3Purity:Min. 95%Molecular weight:233.69 g/mol



