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Benzoic acid, 2-[[(1-acetyl-2,3-dihydro-1H-indol-6-yl)methylamino]sulfonyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849355-52-8

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849355-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849355-52-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,3,5 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 849355-52:
(8*8)+(7*4)+(6*9)+(5*3)+(4*5)+(3*5)+(2*5)+(1*2)=208
208 % 10 = 8
So 849355-52-8 is a valid CAS Registry Number.

849355-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-(1-acetylindolin-6-yl)-N-methyl-2-sulfamoyl benzoate

1.2 Other means of identification

Product number -
Other names 2-[(1-Acetyl-2,3-dihydro-1H-indol-6-yl)-methyl-sulfamoyl]-benzoic acid methyl ester

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:849355-52-8 SDS

849355-52-8Relevant academic research and scientific papers

New antiproliferative benzoindolinothiazepines derivatives

Laconde, Guillaume,Depreux, Patrick,Berthelot, Pascal,Pommery, Nicole,Henichart, Jean-Pierre

, p. 167 - 172 (2007/10/03)

New benzoindolinothiazepines containing a piperazine moiety are described as potent antiproliferative agents against PC3 human prostatic cell lines. This activity could be explained by an accumulation of cells in G1 phase.

Synthesis of substituted benzoindolinothiazepines using 5- And 6-nitroindolines

Laconde,Depreux,Berthelot,Henichart

, p. 39 - 43 (2007/10/03)

The synthesis of benzoindolothiazepine compounds was investigated using Friedel-Crafts reactions conditions from indolines. The amine function of indolinic identity was protected to avoid an alkylation of this function by methyl iodide. It was observed that the treatment of the desired amines with commercially available methyl chlorosulfanoylbenzonate resulted in the formation of sulfonamide compounds. It was also observed that the cyclization of the carboxylic acid under Friedel-Crafts conditions resulted in the formation of the desired tetracycles.

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