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N,N'-(9-Oxo-9H-fluorene-2,7-diyl)bis[1-pyrrolidineacetamide] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64953-57-7

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64953-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64953-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,5 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64953-57:
(7*6)+(6*4)+(5*9)+(4*5)+(3*3)+(2*5)+(1*7)=157
157 % 10 = 7
So 64953-57-7 is a valid CAS Registry Number.

64953-57-7SDS

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 N-[9-oxo-7-[(2-pyrrolidin-1-ylacetyl)amino]fluoren-2-yl]-2-pyrrolidin-1-ylacetamide

1.2 Other means of identification

Product number -
Other names 1-Pyrrolidineacetamide,N,N'-(9-oxo-9H-fluorene-2,7-diyl)bis

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:64953-57-7 SDS

64953-57-7Downstream Products

64953-57-7Relevant academic research and scientific papers

Design, synthesis and antiproliferative evaluation of fluorenone analogs with DNA topoisomerase i inhibitory properties

Lee, Chia-Chung,Chang, Deh-Ming,Huang, Kuo-Feng,Chen, Chun-Liang,Chen, Tsung-Chih,Lo, Yang,Guh, Jih-Hwa,Huang, Hsu-Shan

, p. 7125 - 7133 (2013/11/06)

A series of 2,7-diamidofluorenones were designed, synthesized, and screened by SRB assay. Some synthesized compounds exhibited antitumor activities in submicromolar range. Ten compounds (3a, 3b, 3c, 3g, 3j, 3l, 4a, 4h, 4i, and 4j) were also selected by NCI screening system and 3c (GI50 = 1.66 μM) appeared to be the most active agent of this series. Furthermore, 3c attenuated topoisomerase I-mediated DNA relaxation at low micromolar concentrations. These results indicated that fluorenones have potential to be further developed into anticancer drugs.

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