Fenazox

Fenazox Basic information
Product Name:Fenazox
Synonyms:Amfenac;AMFENAC SODIUM;AMFENAC SODIUM MONOHYDRATE;Amfenac sodium hydrate;2-Amino-3-benzoylbenzeneacetic acid, monosodium salt, monohydrate;Amfenac sodium salt monohydrate;Amfenac Sodium Salt Hydrate;Benzeneacetic acid, 2-amino-3-benzoyl-, sodium salt, monohydrate
CAS:61618-27-7
MF:C15H16NNaO4
MW:297.29
EINECS:1592732-453-0
Product Categories:Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;Inhibitors
Mol File:61618-27-7.mol
Fenazox Structure
Fenazox Chemical Properties
Melting point 242-244°C
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Methanol (Slightly), Water (Slightly)
form Solid
color Yellow
Safety Information
MSDS Information
Fenazox Usage And Synthesis
DescriptionAmfenac sodium is a non-steroidal antiinflammatory agent structurally related to ketoprofen,suprofen(10) and tiaprofenic acid.It is reported to be effective in the short term treatment of rheumatoidarthritis,osteoarthritis and pain associated with minor surgical procedures.
Chemical PropertiesYellow Solid
OriginatorA.H. Robins (USA)
UsesAmfenac is an antibacterial agent
UsesFenazox is used in the synthetic preparation of amides via reductive amidation of esters, which is used in the synthesis of bio-active molecules and natural products.
DefinitionChEBI: A hydrate that is the monohydrate of the sodium salt of amfenac.
Manufacturing Process7-Benzoylindolin-2-one:
Method A. A mixture of 2.5 g (0.0077 mole) of ethyl 2-acetamido-3- benzoylphenylacetate in 50 ml of 3 N hydrochloric acid was refluxed for one hour. The reaction mixture was filtered and the filtrate was poured into a mixture of ice and water. The precipitate was collected and recrystallized from acetone; yield of 7-benzoylindolin-2-one 1 g (55%); melting point 154°C.
Method B. A solution of 1.3 g (0.0044 mole) of 2-acetamido-3- benzoylphenylacetic acid in 15 ml of 3 N hydrochloric acid and 15 ml of acetic acid was refluxed for three hours. The cooled solution was poured into ice water and the 7-benzoylindolin-2-one which precipitated was collected and dried.
2-Amino-3-benzoylphenylacetic acid:
A mixture of 1.0 g (0.004 mole) of 7-benzoylindolin-2-one was added to 30 ml of 3 N sodium hydroxide and the basic solution was refluxed for 45 min under nitrogen. The mixture was filtered and the filtrate was neutralized with glacial acetic acid. The precipitate was filtered off, washed with water and dried. The 2-amino-3-benzoylbenzeneacetic acid melted at 122°C (dec.). The yield was 0.8 g (72%).



Brand nameFENAZOX
Therapeutic FunctionAntiinflammatory
General DescriptionAmfenac (Fenazox), its amide prodrug, nepafenac (Nevanac),and the related analog, bromofenac, are amphoteric becauseof the presence of an additional aromatic amine group.They are less likely to be absorbed into the general circulation.They are approved for use as topical ocular anti-inflammatoryagents for the treatment of postoperative ocular pain,inflammation, and posterior segment edema. The only observedside effects of these drugs are all related to tissuesaround the eye including abnormal ocular sensation, eye rednessand irritation, burning and stinging, and conjunctival orcornea edema.
Fenazox Preparation Products And Raw materials
Raw materialsSodium hydroxide-->Acetic acid-->Hydrochloric acid
Sodium acetate POLY(VINYL ACETATE) Sodium chloride Trisodium phosphate Cellulose acetate Oxamic acid sodium salt Diclofenac sodium ACETATE Ethyl acetate Sodium citrate Sodium bicarbonate P-AMINOBENZAMIDE GLUTAMIC ACID Vinyl acetate Sodium hydroxide L-ACYLASE Ammonium acetate hydrate 1,5-Diphenylcarbazide

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