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2H-Indol-2-one, 7-benzoyl-1,3-dihydro-3-(methylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61085-33-4

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61085-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61085-33-4 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, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61085-33:
(7*6)+(6*1)+(5*0)+(4*8)+(3*5)+(2*3)+(1*3)=104
104 % 10 = 4
So 61085-33-4 is a valid CAS Registry Number.

61085-33-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-benzoyl-3-methylsulfanyl-1,3-dihydroindol-2-one

1.2 Other means of identification

Product number -
Other names 7-benzoyl-3-(methylsulfanyl)-1,3-dihydro-2H-indol-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61085-33-4 SDS

61085-33-4Relevant 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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