| Weight | 245.662 g/mol |
|---|---|
| Formula | C10H12ClNO4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 5 |
CHLORPHENESIN CARBAMATE (886-74-8)
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- THE METABOLISM OF CHLORPHENESIN CARBAMATE (Journal of Pharmacology and Experimental Therapeutics, 1964)
- Comparative Pharmacokinetics of Chlorphenesin Carbamate and Methocarbamol in Man (Journal of Pharmaceutical Sciences, 1971)
- Evaluation of sustained-release granules of chlorphenesin carbamate in dogs and humans (International Journal of Pharmaceutics, 1993)
- The absorption, excretion, and metabolism of chlorphenesin carbamate in the dog (Biochemical Pharmacology, 1966)
- The influence of chlorphenesin carbamate and carisoprodol on psychological test scores. (Current Therapeutic Research-clinical and Experimental, 1969)
- Characterization of the glucuronide conjugate of chlorphenesin carbamate from the rat and from man (Biochemical Pharmacology, 1965)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1OCC(COC(=O)N)O)Cl
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InChIKeySKPLBLUECSEIFO-UHFFFAOYSA-N
- Pubchem - CHLORPHENESIN CARBAMATE
- Wikipedia - chlorphenesin carbamate
Chlorphenesin carbamate (Maolate, Musil) is a centrally acting muscle relaxant used to treat muscle pain and spasms. Chlorphenesin is no longer used for this purpose in most developed nations due to the availability of much safer spasmolytics such as benzodiazepines. It is a naturally occurring compound found in Bull Semen.
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Synthesis
Reactant
+
alpha,4-Dichloroanisole
(Grignard alcohol)
4-Chlorobenzaldehyde
+
Reactant
(Dakin oxidation)
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