CAS 137888-11-0

8-hydroxy-5-[(1R)-1-hydroxy-2-{[(2R)-1-(4-methoxyphenyl)propan-2-yl]amino}ethyl]quinolin-2(1H)-one hydrochloride (1:1)

Description:

8-Hydroxy-5-[(1R)-1-hydroxy-2-{[(2R)-1-(4-methoxyphenyl)propan-2-yl]amino}ethyl]quinolin-2(1H)-one hydrochloride is a complex organic compound characterized by its quinoline core, which is a bicyclic structure containing a nitrogen atom. This substance features multiple functional groups, including a hydroxyl group, an amino group, and a methoxyphenyl moiety, contributing to its potential biological activity. The presence of the hydrochloride indicates that it is a salt form, which can enhance its solubility in water and influence its pharmacokinetic properties. The stereochemistry of the compound is significant, as it contains chiral centers that may affect its interaction with biological targets. This compound is of interest in medicinal chemistry, particularly for its potential therapeutic applications, possibly in the treatment of various diseases. Its specific interactions, efficacy, and safety profile would require further investigation through experimental studies.

Formula: C₂₁H₂₅ClN₂O₄

InChI: InChI=1/C21H24N2O4.ClH/c1-13(11-14-3-5-15(27-2)6-4-14)22-12-19(25)16-7-9-18(24)21-17(16)8-10-20(26)23-21;/h3-10,13,19,22,24-25H,11-12H2,1-2H3,(H,23,26);1H/t13-,19+;/m1./s1

Synonyms:

• 2(1H)-Quinolinone, 8-hydroxy-5-[(1R)-1-hydroxy-2-[[(1R)-2-(4-methoxyphenyl)-1-methylethyl ]amino]ethyl]-, monohydrochloride
• Carmoterol Hydrochloride

Carmoterol Hydrochloride

CAS: 137888-11-0

Stability Hygroscopic
Applications Carmoterol is a highly potent β2-selective adrenoceptor agonist having a long-lasting bronchodilating effect.
References Abagyan, R., et al.: J. Mol. Biol., 235, 983 (1994), Matsukawa, M., et al.: J. Pharm. Biomed. Anal., 17, 245 (1998), Cole, P., et al.: Nat. Chem. Biol., 4, 590 (2008),

Formula: C₂₁H₂₄N₂O₄·ClH

Color and Shape: Yellow To Beige

Molecular weight: 404.89

Ref: TR-C183750