| Weight | 201.697 g/mol |
|---|---|
| Formula | C10H16ClNO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
PSEUDOEPHEDRINE HYDROCHLORIDE (345-78-8)
Pseudoephedrine · Sudafed · Pseudoephedrine HCl
Score:
#1887 in Biology
,
#2274 in Chemistry
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- Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones (Journal of the American Chemical Society, 1997)
- Efficacy and safety of loratadine plus pseudoephedrine in patients with seasonal allergic rhinitis and mild asthma (The Journal of Allergy and Clinical Immunology, 1997)
- Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis (Journal of the American Chemical Society, 1994)
- Impacts of federal ephedrine and pseudoephedrine regulations on methamphetaminerelated hospital admissions (Addiction, 2003)
- Controlled porosity osmotic pump-based controlled release systems of pseudoephedrine: I. Cellulose acetate as a semipermeable membrane (Journal of Controlled Release, 2003)
- Chiral discrimination in the structures and energetics of association of stereoisomeric salts of mandelic acid with .alpha.-phenethylamine, ephedrine, and pseudoephedrine (Journal of the American Chemical Society, 1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Pseudoephedrine
- Sudafed
- Pseudoephedrine HCl
- Isoephedrine
- Threo Isomer of Ephedrine
- Ephedrine Threo Isomer
-
SMILES[H+].CC(C(C1=CC=CC=C1)O)NC.[Cl-]
-
InChIKeyBALXUFOVQVENIU-UHFFFAOYSA-N
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Synthesis
Methylboronic acid
+
Reactant
(Chan-Lam coupling reaction)
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