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104692-85-5

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104692-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104692-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,9 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104692-85:
(8*1)+(7*0)+(6*4)+(5*6)+(4*9)+(3*2)+(2*8)+(1*5)=125
125 % 10 = 5
So 104692-85-5 is a valid CAS Registry Number.

104692-85-5SDS

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 2-chloro-1-[4-(7-chloroquinolin-4-yl)piperazin-1-yl]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:104692-85-5 SDS

104692-85-5Downstream Products

104692-85-5Relevant articles and documents

New derivatives of 7-chloroquinolin-4-amine with antiprotozoal activity

Faist, Johanna,Hinteregger, Clemens,Seebacher, Werner,Saf, Robert,M?ser, Pascal,Kaiser, Marcel,Weis, Robert

, p. 941 - 948 (2017)

Novel ω-aminoacyl and -alkyl derivatives of 7-chloroquinolin-4-amine were prepared and their structures confirmed by NMR spectroscopy. Their antiprotozoal activities were examined in vitro against the sensitive NF54 strain as well as against the multiresistant K1strain of Plasmodium falciparum and against Trypanosoma brucei rhodesiense (STIB 900). The results were compared with the activities of clinically used drugs. Their antitrypanosomal activities were only moderate whereas their antiplasmodial activities looked very promising. Some were equal or slightly more active than chloroquine against the sensitive strain. However, in comparison to chloroquine, the activity of the new compounds was decreased much less in the resistant strain. Several possessed activity against both strains in low nanomolar concentration.

Antiparasitic Agents: Part VI-Synthesis of 7-Chloro-4-(4-substituted-phenylamino)- and 7-Chloro-4-(4-substituted-piperazin-1-yl)quinolines as Potential Antiparasitic Agents

Agrawal, Vijai K.,Sharma, Satyavan

, p. 550 - 555 (2007/10/02)

The synthesis of a series of 7-chloro-4-(4-hydroxy-3-substituted-phenylamino)quinolines (9-13, 31-40, 58) and 7-chloro-4-(4-substituted-piperazin-1-yl)quinolines (41-51, 53-55) has been carried out.These compounds have been tested for their antimalarial,

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