| Weight | 290.794 g/mol |
|---|---|
| Formula | C16H19ClN2O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
carbinoxamine (5560-77-0, 486-16-8)
carbinoxamine maleate · Histex PD · Histex CT
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- Asymmetric synthesis of (S)-carbinoxamine. New aspects of oxazaborolidine-catalyzed enantioselective carbonyl reduction (Tetrahedron Letters, 1996)
- Stereochemical aspects of antihistamine action. 4. Absolute configuration of carbinoxamine antipodes. (Journal of Medicinal Chemistry, 1971)
- Ion Exchange Resin Salts for Oral Therapy I: Carbinoxamine (Journal of Pharmaceutical Sciences, 1962)
- Quantitative chiral analysis of carbinoxamine, doxylamine, and orphenadrine by capillary zone electrophoresis (Journal of Microcolumn Separations, 2000)
- Capillary GLC Assay for Carbinoxamine and Hydrocodone in Human Serum Using Nitrogen-Sensitive Detection (Journal of Pharmaceutical Sciences, 1983)
- Spectrophotometric Determination of the Antihistamines, Carbinoxamine Maleate and Doxylamine Succinate, in an N-Cetylpyridinium Chloride Micellar Medium (Analytical Letters, 1996)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - carbinoxamine maleate
- Histex PD
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- Histex I-E
-
SMILESCN(C)CCOC(C1=CC=C(C=C1)Cl)C2=CC=CC=N2
-
InChIKeyOJFSXZCBGQGRNV-UHFFFAOYSA-N
- Pubchem - carbinoxamine
- Wikipedia - carbinoxamine
Carbinoxamine (Clistin, Palgic, Rondec, Rhinopront) is a antihistamine and anticholinergic agent. It was first launched in the United States by the McNeil Corporation under the brand name Clistin. It is now available under the brand name Palgic as 4 mg tablets or 4 mg/5 mL liquid.
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Synthesis
CHLOROBENZENE
+
Reactant
(Friedel-Crafts alkylation)
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