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99532-51-1

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99532-51-1 Usage

General Description

1-(Phenylsulfonyl)-1H-indole-3-carbonyl chloride is a chemical compound that contains a phenylsulfonyl group and a carbonyl chloride group attached to an indole ring. It is commonly used in organic synthesis as a reagent for the introduction of carbonyl chloride functionality into various organic molecules. 1-(PHENYLSULFONYL)-1H-INDOLE-3-CARBONYL CHLORIDE is known for its ability to react with a wide range of nucleophiles, making it useful in the production of diverse organic compounds. It is also utilized in the pharmaceutical industry for the synthesis of potential drug candidates and in the development of new materials and compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 99532-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,3 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99532-51:
(7*9)+(6*9)+(5*5)+(4*3)+(3*2)+(2*5)+(1*1)=171
171 % 10 = 1
So 99532-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClNO3S/c16-15(18)13-10-17(14-9-5-4-8-12(13)14)21(19,20)11-6-2-1-3-7-11/h1-10H

99532-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfonyl)indole-3-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 3-(chlorocarbonyl)-1-(phenylsulfonyl)-1H-indole

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:99532-51-1 SDS

99532-51-1Relevant articles and documents

Synthesis and biological evaluation of bengacarboline derivatives

Pouilhes, Annie,Kouklovsky, Cyrille,Langlois, Yves,Baltaze, Jean-Pierre,Vispe, Stephane,Annereau, Jean-Philippe,Barret, Jean-Marc,Kruczynski, Anna,Bailly, Christian

, p. 1212 - 1216 (2008/12/21)

Novel derivatives of the marine alkaloid bengacarboline have been synthesized. The seco derivatives 11 and 12 were evaluated for topoisomerase inhibition, DNA damages, cytotoxicity and cell cycle perturbation. The two synthetic analogs are more potent cyt

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