| Weight | 275.776 g/mol |
|---|---|
| Formula | C13H22ClNO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
Levalbuterol hydrochloride (148563-16-0, 50293-90-8)
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- Sigma-Aldrich - Levalbuterol hydrochloride84.60 - 338.10 USD
- Fisher Scientific - Search for Levalbuterol hydrochloride
- TCI - Search for Levalbuterol hydrochloride
- Levalbuterol hydrochloride polymorph a (2005)
- Levalbuterol hydrochloride polymorphic b (2005)
- Analysis of levalbuterol hydrochloride sustained release capsules by RP-HPLC (Journal of Guangdong Pharmaceutical College, 2009)
- Preparation of levalbuterol hydrochloride (2005)
- Study on Preparation of Levalbuterol Hydrochloride and Racemization of S-Enantiomer (The Chinese Pharmaceutical Journal, 2007)
- Determination of levalbuterol hydrochloride by HPLC (The Chinese Pharmaceutical Journal, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)NCC(C1=CC(=C(C=C1)O)CO)O.Cl
-
InChIKeyOWNWYCOLFIFTLK-UHFFFAOYSA-N
- Pubchem - Levalbuterol hydrochloride
- Wikipedia - levalbuterol hydrochloride
Levosalbutamol, also known as levalbuterol, is a short-acting 2 adrenergic receptor agonist used in the treatment of asthma and chronic obstructive pulmonary disease (COPD). Evidence does not show that levosalbutamol works better than salbutamol, thus there may not be sufficient justification for prescribing it. The drug is the (R)-()-enantiomer of its prototype drug salbutamol.
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Alternate Names
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Synthesis
Reactant
+
5330-38-1
(Grignard alcohol)
Reactant
+
tert-Butylamine
(Reductive amination)
Reactant
+
2-Chloro-2-methylpropane
(Alkylation of primary amines)
salicyl alcohol
+
Reactant
(Friedel-Crafts alkylation)
Tert-butylboronic Acid
+
Reactant
(Chan-Lam coupling reaction)
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Levalbuterol hydrochloride
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