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7-benzoyl-5-methoxyindolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61085-29-8

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61085-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61085-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61085-29:
(7*6)+(6*1)+(5*0)+(4*8)+(3*5)+(2*2)+(1*9)=108
108 % 10 = 8
So 61085-29-8 is a valid CAS Registry Number.

61085-29-8Relevant academic research and scientific papers

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.

4-(5- And 7-)benzoylindolin-2-ones and pharmaceutical uses thereof

-

, (2008/06/13)

Novel 4-(5- and 7-)benzoylindolin-2-ones of the formula: SPC1 Wherein R is hydrogen, lower-alkyl, or methylthio, R1 is hydrogen or lower-alkyl, R2 is lower-alkyl, lower-alkoxy, halogen, nitro or trifluoromethyl, R3 is hydrogen, halogen or lower-alkoxy, and n is 0, 1 or 2, are prepared by (a) acylation of indolin-2-one to give 5-benzoylindoline-2-one, (b) cyclization of 2-acetamido-3-benzoylphenylacetic acid or ethyl 2-acetamido-3-benzoylphenylacetate to give 7-benzoyindoline-2-one, or (c) by reacting aminobenzophenones with alkyl α(methylthio)acetates to give alkyl 2-amino-3-(5- or 6-)benzoyl-α-(methylthio)phenylacetates which are cyclized and demethylthiolated to 4-(5- and 7-)benzoylindolin-2-ones. The novel compounds possess anti-inflammatory activity and are intermediates for the preparation of 2-amino-3-(5- or 6-) benzoylphenylacetic acids which posess anti-inflammatory properties.

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