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303-79-7

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303-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 303-79-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 303-79:
(5*3)+(4*0)+(3*3)+(2*7)+(1*9)=47
47 % 10 = 7
So 303-79-7 is a valid CAS Registry Number.

303-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-10-oxidophenazin-5-ium 5-oxide

1.2 Other means of identification

Product number -
Other names 2-Chlorphenazin-5,10-dioxid

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:303-79-7 SDS

303-79-7Relevant articles and documents

Double-strand cleavage of DNA by a polyamide-phenazine-di-N-oxide conjugate

Zhou, Hang,Gao, Juanhong,Chen, Zhaohang,Duan, Shan,Li, Chao,Qiao, Renzhong

, p. 284 - 288 (2018/01/03)

Phenazine and its derivatives have been widely applied as nucleic acid cleavage agents due to active oxygen activating the C–H bond of the substrate. However, diffusion of oxygen radicals limits their potential applications in the DNA-targeted metal-free drug. Introduction of groove binder moiety such as polyamide enhanced the regional stability of radical molecules and reduced cytotoxicity of the drugs. In this work, we described the design and synthesis of a polyamide-modified phenazine-di-N-oxide as a DNA double-strand cleavage agent. The gel assays showed the hybrid conjugates can effectively break DNA double strands in a non-random manner under physiological conditions. The probable binding mode to DNA was investigated by sufficient spectral experiments, revealing weak interaction between hybrid ligand and nucleic acid molecules. The results of our study have implications on the design of groove-binding hybrid molecules as new artificial nucleases and may provide a strategy for developing efficient and safe DNA cleavage reagents.

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