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2-Imidazolidinone, 1-[(4-amino-3-chlorophenyl)sulfonyl]-4-phenyl-, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

823786-86-3

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823786-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 823786-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,3,7,8 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 823786-86:
(8*8)+(7*2)+(6*3)+(5*7)+(4*8)+(3*6)+(2*8)+(1*6)=203
203 % 10 = 3
So 823786-86-3 is a valid CAS Registry Number.

823786-86-3SDS

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 (4S)-1-(4-amino-3-chlorophenyl)sulfonyl-4-phenylimidazolidin-2-one

1.2 Other means of identification

Product number -
Other names -

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:823786-86-3 SDS

823786-86-3Downstream Products

823786-86-3Relevant academic research and scientific papers

Novel diarylsulfonylurea derivatives as potent antimitotic agents

Kim, Semi,Park, Ji Hyun,Koo, Sun-Young,Kim, Jung In,Kim, Min-Hyeung,Kim, Ji Eun,Jo, Kiwon,Geun Choi, Hwan,Lee, Sung Bae,Jung, Sang-Hun

, p. 6075 - 6078 (2007/10/03)

Novel diarylsulfonylurea derivatives have been synthesized and identified as potent inhibitors of tubulin polymerization and cancer cell proliferation. Furthermore, these compounds were also efficacious against multidrug-resistant cancer cells. A novel series of diarylsulfonylurea derivatives were synthesized and evaluated for interaction with tubulin and for cytotoxicity against human cancer cell lines. These derivatives demonstrated good inhibitory activity against tubulin polymerization, which was well correlated with promising antiproliferative activity as well as G2/M phase cell cycle arrest. Furthermore, several compounds were also efficacious against multidrug-resistant cancer cells, which are resistant to many other known microtubule inhibitors.

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