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Ethanone, 1-[4-[[4,6-bis[(4-bromophenyl)amino]-1,3,5-triazin-2-yl]amino]phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84688-79-9

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84688-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84688-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,8 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84688-79:
(7*8)+(6*4)+(5*6)+(4*8)+(3*8)+(2*7)+(1*9)=189
189 % 10 = 9
So 84688-79-9 is a valid CAS Registry Number.

84688-79-9SDS

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 1-{4-[4,6-Bis-(4-bromo-phenylamino)-[1,3,5]triazin-2-ylamino]-phenyl}-ethanone

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:84688-79-9 SDS

84688-79-9Downstream Products

84688-79-9Relevant academic research and scientific papers

Triaminotriazine DNA helicase inhibitors with antibacterial activity

McKay, Geoffrey A.,Reddy, Ranga,Arhin, Francis,Belley, Adam,Lehoux, Dario,Moeck, Greg,Sarmiento, Ingrid,Parr, Thomas R.,Gros, Philippe,Pelletier, Jerry,Far, Adel Rafai

, p. 1286 - 1290 (2007/10/03)

Screening of a chemical library in a DNA helicase assay involving the Pseudomonas aeruginosa DnaB helicase provided a triaminotriazine inhibitor with good antibacterial activity but associated cytotoxicity toward mammalian cells. Synthesis of analogs provided a few inhibitors that retained antibacterial activity and demonstrated a significant reduction in cytotoxicity. The impact of serum and initial investigations toward a mode of action highlight several features of this class of compounds as antibacterials.

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