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5,6-Quinolinediol, 8-((5-((1-methylethyl)amino)pentyl)amino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17605-76-4

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17605-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17605-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17605-76:
(7*1)+(6*7)+(5*6)+(4*0)+(3*5)+(2*7)+(1*6)=114
114 % 10 = 4
So 17605-76-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H25N3O2/c1-12(2)18-8-4-3-5-9-19-14-11-15(21)17(22)13-7-6-10-20-16(13)14/h6-7,10-12,18-21H,3-5,8-9H2,1-2H3

17605-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-(5-isopropylamino-pentylamino)-quinoline-5,6-diol

1.2 Other means of identification

Product number -
Other names 8-(5-Isopropylamino-pentylamino)-quinoline-5,6-diol

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:17605-76-4 SDS

17605-76-4Downstream Products

17605-76-4Relevant academic research and scientific papers

8-Aminoquinolines as anticoccidials - I

Armer, Richard E.,Barlow, Jacqueline S.,Dutton, Christopher J.,Greenway, David H.J.,Greenwood, Sean D.W.,Lad, Nita,Tommasini, Ivan

, p. 2585 - 2588 (2007/10/03)

The proposed ring metabolites of the 8-aminoquinoline antimalarial, pentaquine, 1, have been synthesised and their biological activity as anticoccidial agents investigated in vivo. Several analogues in which this metabolic pathway had been blocked were also synthesised and their anticoccidial activity measured.

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