ChemicalBook--->CAS DataBase List--->118-57-0

118-57-0

118-57-0 Structure

118-57-0 Structure
IdentificationBack Directory
[Name]

2-HYDROXYBENZOIC ACID 4-(ACETYLAMINO)PHENYL ESTER
[CAS]

118-57-0
[Synonyms]

SALOPHEN
Asalphen
Cetosalol
Phenestal
Phenetsal
acetaminosalol
p-Acetamidophenyl salicylate
4-acetamidophenyl salicylate
4-Acetaminophenyl salicylate
ACETYL-P-AMINOPHENYLSALICYLATE
Salicylic acid 4-(acetylamino)phenyl
(4-acetamidophenyl) 2-hydroxybenzoate
Salicylic acid 4-(acetylamino)phenyl ester
2-hydroxybenzoic acid (4-acetamidophenyl) ester
2-HYDROXYBENZOIC ACID 4-(ACETYLAMINO)PHENYL ESTER
[EINECS(EC#)]

204-261-3
[Molecular Formula]

C15H13NO4
[MDL Number]

MFCD00020033
[MOL File]

118-57-0.mol
[Molecular Weight]

271.27
Chemical PropertiesBack Directory
[Appearance]

solid
[Melting point ]

187°
[Stability:]

Stable. Incompatible with strong oxidizing agents.
[LogP]

2.562 (est)
Hazard InformationBack Directory
[Chemical Properties]

solid
[Originator]

Acetaminosal ,ZYF Pharm Chemical
[Uses]

Analgesic; antipyretic.
[Definition]

ChEBI: Acetaminosalol is a carbonyl compound.
[Manufacturing Process]

2 Methods of producing of acetyl salicylic acid ester of N-acetyl-paminophenol:
1. 65.0 g of N-acetyl-p-aminophenol were slurried with 400 ml of water and cooled to 10°C. 125 ml of 20% sodium hydroxide were slowly added to the mixture with stirring, the temperature being maintained 10°-15°C. To the solution obtained, 75.0 g of acetyl salicylic chloride were added with vigorous stirring over a period of 0.5 h, the solution being maintained at a temperature of about 10°C. Towards the end of the reaction the pH was checked and adjusted to greater than 10 by the addition of a small amount of 20% sodium hydroxide. After all the acid chloride had been added, vigorous stirring was continued for 0.5 h during which time the crude product separated out. The acetyl salicylic acid ester of N-acetyl-p-aminophenol was filtered off, washed thoroughly with water and recrystallised from ethanol.
2. 65.0 g of sodium N-acetyl-p-aminophenol were slurried with 500.0 g of dry benzene and 80.0 g of acetyl salicylic chloride added. The mixture was heated under reflux for 4 h and filtered hot. The excess benzene was removed under vacuum and the crude acetyl salicylic acid ester of N-acetyl-p-aminophenol crystallized from ethanol.
[Brand name]

Acephen (G & W); Infants’ Feverall (Actavis); Injectapap (Ortho-McNeil); Neopap (Polymedica); Tylenol (McNeil).
[Therapeutic Function]

Analgesic, Antineuralgic, Antirheumatic, Antipyretic
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