Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate

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1.What is the Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate ?

Bromfenac is a non-steroidal anti-inflammatory agent.

2.What is the CAS number for Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate ?

The CAS number of Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate is 120638-55-3.

More information of Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate 120638-55-3 are:

3.What are another words for Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate ?

Synonyms?for?Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate 120638-55-3:Benzeneaceticacid, 2-amino-3-(4-bromobenzoyl)-, monosodium salt, hydrate (2:3) (9CI);Benzeneacetic acid,2-amino-3-(4-bromobenzoyl)-, sodium salt, hydrate (2:2:3);

4.What is the molecular formula of Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate?

The chemical formula of ?Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate is?C15H12BrNO3 . 3/2 H2O . Na which containing 15 Carbon atoms,14 Hydrogen atoms,1 Bromine atoms,1 Nitrogen atoms,1 Oxygen atoms and 1 Sodium atoms,and the molecular weight of??Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate?is 334.16500.

5.What is Sodium (2-amino-3-(4-bromobenzoyl)phenyl)acetate (120638-55-3) used for?

Duract was launched in the US as a potent, orally-active, long lasting peripheral analgesic with antiinflammatory properties. It is structurally similar to ketoprofen and diclofenac and can be prepared in three steps from 2-amino-4’-bromophenone using Gassman’s oxindole synthesis. Duract’s biological effects are a result of its ability to reduce prostaglandin production through inhibition of cyclooxygenase. As a 4-bromo derivative of Amfenac, this modification increased the duration of analgesic activity and antiinflammatory potency. It was also free of any CNS, cardiovascular or autonomic effects. In comparison, 5 mg of Duract was equipotent to 650 mg of ASA and 25 mg was slightly more potent than 400 mg of Ibuprofen.

InChI:InChI=1/C15H12BrNO3.Na.H2O/c16-11-6-4-9(5-7-11)15(20)12-3-1-2-10(14(12)17)8-13(18)19;;/h1-7H,8,17H2,(H,18,19);;1H2/q;+1;/p-1

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