amfenac

Product Name
amfenac
CAS No.
51579-82-9
Chemical Name
amfenac
Synonyms
SOYCMDCMZDHQFP-UHFFFAOYSA-N;Nepafenac Impurity 5(Amfenac);2-Amino-3-benzoylbenzeneacetic acid;Benzeneacetic acid, 2-amino-3-benzoyl-;Amfenac D5Q: What is Amfenac D5 Q: What is the CAS Number of Amfenac D5 Q: What is the storage condition of Amfenac D5 Q: What are the applications of Amfenac D5
CBNumber
CB71357722
Molecular Formula
C15H13NO3
Formula Weight
255.27
MOL File
51579-82-9.mol
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amfenac Property

Melting point:
121-123° (dec)
Boiling point:
398.5°C (rough estimate)
Density 
1.1654 (rough estimate)
refractive index 
1.5500 (estimate)
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Safety

Toxicity
LD50 in mice, rats (mg/kg): 615, 311 orally (Sancilio)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
API0016452
Product name
AMFENAC
Purity
95.00%
Packaging
5MG
Price
$504.1
Updated
2021/12/16
AvaChem
Product number
2872A
Product name
Amfenac
Packaging
100mg
Price
$29
Updated
2021/12/16
AvaChem
Product number
2872A
Product name
Amfenac
Packaging
1g
Price
$45
Updated
2021/12/16
AvaChem
Product number
2872A
Product name
Amfenac
Packaging
10g
Price
$245
Updated
2021/12/16
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amfenac Chemical Properties,Usage,Production

Originator

Amfenac sodium,Yungjin Pharmacetical Co. Ltd.

Uses

Anti-inflammatory.

Definition

ChEBI: An oxo monocarboxylic acid that is benzophenone in which one of the phenyl groups is substituted by an amino group and a carboxymethyl group at position 2 and 3, respectively. The corresponding carboxamide, nepafenac, is a prodrug of amfenac and is used fo the treatment of pain and inflammation following cataract surgery.

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%).

Therapeutic Function

Antiinflammatory

amfenac Preparation Products And Raw materials

Raw materials

Preparation Products

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amfenac Suppliers

BOC Sciences
Tel
1-631-485-4226; 16314854226
Email
info@bocsci.com
Country
United States
ProdList
14059
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65
SynAsst Chemical.
Tel
021-60343070
Fax
021-35122006
Country
China
ProdList
12742
Advantage
55
TargetMol Chemicals Inc.
Tel
021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7934
Advantage
58
ChemStrong Scientific Co.,Ltd
Tel
0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
17982
Advantage
56
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9926
Advantage
65
Shenzhen SUNGENING Bio-Medical Co., Ltd.
Tel
0755-28967200 13631290199
Fax
0755-28967200
Email
wxf@sungening.com
Country
China
ProdList
9506
Advantage
60
Shenzhen Regent Biochemical Technology Co., Ltd.
Tel
0755-0755-85201366 18938635012
Fax
0755-85201366
Email
sales@regentsciences.com
Country
China
ProdList
9287
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 13028896684
Email
sales@rrkchem.com
Country
China
ProdList
55672
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58
Accela ChemBio Inc.
Tel
(+1)-858-699-3322
Fax
(+1)-858-876-1948
Email
info@accelachem.com
Country
United States
ProdList
19965
Advantage
58

51579-82-9, amfenacRelated Search:


  • 2-Amino-3-benzoylbenzeneacetic acid
  • SOYCMDCMZDHQFP-UHFFFAOYSA-N
  • Nepafenac Impurity 5(Amfenac)
  • Benzeneacetic acid, 2-amino-3-benzoyl-
  • Amfenac D5Q: What is Amfenac D5 Q: What is the CAS Number of Amfenac D5 Q: What is the storage condition of Amfenac D5 Q: What are the applications of Amfenac D5
  • 51579-82-9