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126362-91-2

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  • 3-Quinolinecarboxylic acid, 1-(4-aminophenyl)-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-

    Cas No: 126362-91-2

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126362-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126362-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,6 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126362-91:
(8*1)+(7*2)+(6*6)+(5*3)+(4*6)+(3*2)+(2*9)+(1*1)=122
122 % 10 = 2
So 126362-91-2 is a valid CAS Registry Number.

126362-91-2SDS

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 A 60916

1.2 Other means of identification

Product number -
Other names 3-Quinolinecarboxylic acid, 1-(4-aminophenyl)-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-

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:126362-91-2 SDS

126362-91-2Downstream Products

126362-91-2Relevant articles and documents

SYNTHESIS OF SOME 1-ARYL-1,4-DIHYDRO-4-OXOQUINOLINE-3-CARBOXYLIC ACIDS AND THEIR ANTIBACTERIAL ACTIVITY

Radl, Stanislav,Zikan, Viktor

, p. 2181 - 2189 (2007/10/02)

1,4-Dihydro-4-oxoquinoline-3-carboxylic acids VIIIc and VIIId were prepared via their ethyl esters VIIIa and VIIIb, which were obtained by a direct arylation of ethyl 7-chloro-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate (VIa).When treated with piperazine or N-methylpiperazine compound VIIId yields VIIIe or VIIIf, respectively.Reduction of VIIId, VIIIe, and VIIIf with ferrous sulfate yields VIIIg, VIIIh, and VIIIi respectively.Diazotization and introduction of fluorine into VIIIg using hydrogen fluoride-pyridine yields VIIIj.The compounds prepared were testedfor their antimicrobial activity in vitro.

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