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6-BENZOYLOXINDOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91713-63-2

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91713-63-2 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 27, p. 1379, 1984 DOI: 10.1021/jm00377a001

Check Digit Verification of cas no

The CAS Registry Mumber 91713-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,1 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91713-63:
(7*9)+(6*1)+(5*7)+(4*1)+(3*3)+(2*6)+(1*3)=132
132 % 10 = 2
So 91713-63-2 is a valid CAS Registry Number.

91713-63-2SDS

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 6-benzoyl-1,3-dihydroindol-2-one

1.2 Other means of identification

Product number -
Other names 6-BENZOYLOXINDOLE

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:91713-63-2 SDS

91713-63-2Relevant academic research and scientific papers

An improved procedure for the regiospecific synthesis of electron deficient 4- and 6-substituted isatins

Kraynack, Erica A.,Dalgard, Jackline E.,Gaeta, Federico C. A.

, p. 7679 - 7682 (2007/10/03)

The regiospecific synthesis of 4- and 6-substituted isatins 5a-g in four steps from halonitrobenzenes 1a-g has been investigated for a variety of substrates (Scheme 1). The procedure makes use of readily available, easily handled materials and in most cases purification of neither intermediates nor final products is required. Yields of isatins are between 26 and 75% (Table 1). Improved yields of known isatins are reported as well as the syntheses of previously unreported isatins. This method, taken together with known procedures, provides for the synthesis of the full complement of isatin regioisomers.

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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