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Fenazox

CAS No.
61618-27-7
Chemical Name:
Fenazox
Synonyms
Fenazox;Amfenac;NSC 309467;AMFENAC SODIUM;acetate hydrate;Fenazox USP/EP/BP;Amfenac Sodium Salt;Sodium aminophenate;Amfenac sodium hydrate;Amfenac-d5 Sodium Salt
CBNumber:
CB5969698
Molecular Formula:
C15H16NNaO4
Molecular Weight:
297.29
MDL Number:
MFCD09842317
MOL File:
61618-27-7.mol
Last updated:2024-03-19 15:37:50

Fenazox 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
FDA UNII PPF9V8J28Y

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338

Fenazox price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC A576500 AmfenacSodiumHydrate 61618-27-7 50mg $80 2021-12-16 Buy
TRC A576500 AmfenacSodiumHydrate 61618-27-7 100mg $115 2021-12-16 Buy
Biosynth Carbosynth FA17348 Amfenac sodium salt hydrate 61618-27-7 2g $120 2021-12-16 Buy
Matrix Scientific 094811 Sodium 2-(2-amino-3-benzoylphenyl)acetate hydrate 95+% 61618-27-7 5g $147 2021-12-16 Buy
AK Scientific J52642 Amfenacsodiummonohydrate 61618-27-7 5g $150 2021-12-16 Buy
Product number Packaging Price Buy
A576500 50mg $80 Buy
A576500 100mg $115 Buy
FA17348 2g $120 Buy
094811 5g $147 Buy
J52642 5g $150 Buy

Fenazox Chemical Properties,Uses,Production

Description

Amfenac 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 Properties

Yellow Solid

Originator

A.H. Robins (USA)

Uses

Amfenac is an antibacterial agent

Uses

Fenazox 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.

Definition

ChEBI: A hydrate that is the monohydrate of the sodium salt of amfenac.

Manufacturing Process

7-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 name

FENAZOX

Therapeutic Function

Antiinflammatory

General Description

Amfenac (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.

Synthesis

The reaction of 1-aminoindolin- 2-one with phenylacetone in presence of acetic acid in refluxing ethanol gives 1-(α- methylphenethylidieneimino)indolin-2-one, which by reaction with refluxing ethanolic hydrogen chloride affords ethyl α-(2-methyl- 3-phenylindol-7-yl)acetate. The ozonolysis of this intermediate in acetic acid yields ethyl 2- acetamido-3-benzoylphenyl acetate, which is cyclized by refluxing with HCl in acetic acid to give 7-benzoylindolin-2-one. Alternatively, the hydrolysis of the ester ethyl α-(2-methyl-3- phenylindol-7-yl)acetate with KOH in refluxing water affords the corresponding acid, which can be ozonolyzed as before yielding 2-acetamido- 3-benzoylphenylacetic acid. This acid can be cyclized to 7-benzoyl-1,3-dihydro-indol-2-one by refluxing with HCl in acetic acid as before .

Fenazox Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 187)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Shanghai Time Chemicals CO., Ltd.
+86-021-57951555 +8617317452075 jack.li@time-chemicals.com China 1807 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19553 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58

View Lastest Price from Fenazox manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Amfenac sodium/Fenazox pictures 2021-09-29 Amfenac sodium/Fenazox
61618-27-7
US $0.00-0.00 / Kg/Drum 1KG 98.5%min 500kg WUHAN FORTUNA CHEMICAL CO., LTD
Fenazox pictures 2021-07-13 Fenazox
61618-27-7
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
Fenazox pictures 2021-07-09 Fenazox
61618-27-7
US $15.00-10.00 / KG 1KG 99%+ HPLC Monthly supply of 1 ton Zhuozhou Wenxi import and Export Co., Ltd
  • Fenazox pictures
  • Fenazox
    61618-27-7
  • US $15.00-10.00 / KG
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd
  • Fenazox pictures
  • Fenazox
    61618-27-7
  • US $15.00-10.00 / KG
  • 99%+ HPLC
  • Zhuozhou Wenxi import and Export Co., Ltd

Fenazox Spectrum

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 Fenazox Sodium 2-(2-amino-3-benzoylphenyl)acetate hydrate 2-AMino-3-benzoylbenzeneacetic Acid SodiuM Salt Hydrate NSC 309467 Benzeneacetic acid, 2-amino-3-benzoyl-, sodium salt, hydrate (1:1:1) Amfenac sodium hydrate, >=99% AMfenac sodiuM(Fenazox) Amfenac Sodium Salt acetate hydrate Sodium 2-(2-amino-3-benzoylphenyl) Benzeneacetic acid, 2-amino-3-benzoyl-, monosodium salt,monohydrate Fenazox USP/EP/BP Amfenac-d5 Sodium Salt Amfenac Sodium SaltQ: What is Amfenac Sodium Salt Q: What is the CAS Number of Amfenac Sodium Salt Q: What is the storage condition of Amfenac Sodium Salt Sodium aminophenate 61618-27-7 6168-27-7 C15H14NNaO4 C15H12NNaO3H2O C15H12NO3H2ONa C15H12NO3Na C15H12NO3NaH2O Amines Aromatics Intermediates & Fine Chemicals Pharmaceuticals Inhibitors