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2H-Indol-2-one, 7-(4-fluorobenzoyl)-1,3-dihydro-5-methyl- is a complex organic compound with the molecular formula C16H13FNO2. It is a derivative of indole-2-one, featuring a 4-fluorobenzoyl group attached to the 7-position and a methyl group at the 5-position. 2H-Indol-2-one, 7-(4-fluorobenzoyl)-1,3-dihydro-5-methyl- is characterized by its unique structure, which includes a dihydro-indole core and a fluorinated aromatic ring. It is synthesized through a series of chemical reactions and is typically used in the field of organic chemistry for various applications, such as the synthesis of pharmaceuticals or other complex organic molecules. The compound's properties, such as its reactivity and stability, are influenced by the presence of the fluorine atom and the dihydro-indole structure, making it a potentially interesting candidate for further chemical exploration and development.

83388-22-1

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83388-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83388-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,8 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83388-22:
(7*8)+(6*3)+(5*3)+(4*8)+(3*8)+(2*2)+(1*2)=151
151 % 10 = 1
So 83388-22-1 is a valid CAS Registry Number.

83388-22-1Relevant academic research and scientific papers

2-Amino-3-(alkylthiobenzoyl)-phenylacetic acids

-

, (2008/06/13)

Novel 2-amino-3-(alkylthiobenzoyl)phenylacetic acids, esters and metal salts have the formula: STR1 wherein R is hydrogen or lower alkyl, R1 is hydrogen, lower alkyl or pharmaceutically acceptable metal cation, R2 is hydrogen, haloge

Antiinflammatory agents. 3. Synthesis and pharmacological evaluation of 2-amino-3-benzoylphenylacetic acid and analogues

Walsh,Moran,Shamblee,Uwaydah,Welstead Jr.,Sancilio,Dannenburg

, p. 1379 - 1388 (2007/10/02)

A series of substituted derivatives of 2-amino-3-benzoylphenylacetic acid (amfenac) has been synthesized and evaluated for antiinflammatory, analgesic, and cyclooxygenase inhibiting activity. Several derivatives including 4'-chloro, 4'-bromo and 5-chloro, 4'-bromo were more potent than indomethacin in these assays.

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