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"N~4~-(7-chloro-3-methylquinolin-4-yl)-N~1~,N~1~-diethylpentane-1,4-diamine" is a complex organic compound with the molecular formula C~20~H~27~ClN~4~. It features a quinoline ring system, which is a tricyclic aromatic structure, with a chlorine atom at the 7-position and a methyl group at the 3-position. The compound is characterized by two ethylamine groups attached to the 1-position of the quinoline, and a pentane-1,4-diamine chain connecting these two ethylamine groups. This structure suggests that the compound may have potential applications in medicinal chemistry or as a chemical intermediate due to its unique combination of functional groups and aromatic systems.

85-10-9

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85-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85-10-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85-10:
(4*8)+(3*5)+(2*1)+(1*0)=49
49 % 10 = 9
So 85-10-9 is a valid CAS Registry Number.

85-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylchloroquine

1.2 Other means of identification

Product number -
Other names N4,N4-diethyl-N1-(7-chloro-3-methyl-[4]quinolyl)-1-methyl-butanediyldiamine

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:85-10-9 SDS

85-10-9Downstream Products

85-10-9Relevant academic research and scientific papers

Antimalarials: Synthesis of 4-aminoquinolines that circumvent drug resistance in malaria parasites

De,Byers,Krogstad

, p. 315 - 320 (2007/10/03)

The strategies described here have permitted the synthesis of a series of 4-aminoquinoline antimalarials. Substantive improvements over previous syntheses include nucleophilic substitution with neat amine rather than in phenol, regioselective reductive alkylation to convert the terminal primary amine (12a-20a) on the diaminoalkane side chain to a diethylamino group, and purification by column chromatography with basic alumina. The 1H nmr spectra obtained after regioselective reductive alkylation with sodium borodeuteride (in comparison with sodium borohydride) demonstrated that this reductive alkylation proceeds via formation and subsequent reduction of the corresponding diamides in situ.

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