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chlorthenoxazine

Product Name
chlorthenoxazine
CAS No.
132-89-8
Chemical Name
chlorthenoxazine
Synonyms
Ap 67;Valtorin;Valmorin;Piroxina;Ossazone;Apirazin;chlorthenoxazin;chlorthenoxazine;Chlorethylbenzmethoxazone;Chlorthenoxazine,inhibit,Inhibitor
CBNumber
CB9899858
Molecular Formula
C12H8ClNO
Formula Weight
217.65102
MOL File
132-89-8.mol
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chlorthenoxazine Property

Melting point:
146-147° (dec)
Boiling point:
303°C (rough estimate)
Density 
1.2414 (rough estimate)
refractive index 
1.5500 (estimate)
storage temp. 
Store at -20°C
solubility 
Soluble in DMSO
pka
12.70±0.40(Predicted)
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Hazard and Precautionary Statements (GHS)

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chlorthenoxazine Chemical Properties,Usage,Production

Originator

Reugaril ,Farber ,Italy ,1966

Definition

ChEBI: Chlorthenoxazine is a benzoxazine.

Manufacturing Process

A mixture of 4 liters chloroform and 1,050 cc ethanol was saturated with dry hydrogen chloride gas at -5°C to +5°C in a vessel having a net volume of 15 liters and provided with a stirring device, reflux cooler, gas feed line, thermometer and dropping funnel. 455 g acrolein which had been precooled to 0°C were added dropwise to the solution over a period of 1 to 2 hours while maintaining the temperature below +5°C and vigorously stirring. 1,070 g salicylamide and 1,080 g glacial acetic acid were added to the resulting solution of beta-chloropropionaldehyde acetal, thereby forming a suspension which was heated to 60°C while stirring. A clear solution was formed which was maintained at 60°C for an additional hour. The solution was allowed to cool to about 40°C and was then washed with water by passing a strong stream of water under the surface of the chloroform and continuously withdrawing the upper phase. When the water had reached a pH of 3-4, the precipitated reaction product was separated by vacuum filtration. The chloroform phase of the filtrate was evaporated under a weak vacuum and the residue was combined with the precipitate first obtained. The combined products were stirred with 2 liters of a 5% sodium hydroxide solution. The raw reaction product was then washed with water, dried and recrystallized from ethanol. The product had the melting point of 146°C to 147°C (decomposition). The yield was 1,260 g, corresponding to 76% of the theoretical yield.

Therapeutic Function

Antipyretic, Analgesic

chlorthenoxazine Preparation Products And Raw materials

Raw materials

Preparation Products

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chlorthenoxazine Suppliers

TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
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