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105956-97-6

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105956-97-6 Usage

Uses

Different sources of media describe the Uses of 105956-97-6 differently. You can refer to the following data:
1. Antibacterial.
2. Clinafloxacin is a fluoroquinolone that inhibits both DNA gyrase and topoisomerase IV.

Check Digit Verification of cas no

The CAS Registry Mumber 105956-97-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,9,5 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105956-97:
(8*1)+(7*0)+(6*5)+(5*9)+(4*5)+(3*6)+(2*9)+(1*7)=146
146 % 10 = 6
So 105956-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H17ClFN3O3/c18-13-14-10(5-12(19)15(13)21-4-3-8(20)6-21)16(23)11(17(24)25)7-22(14)9-1-2-9/h5,7-9H,1-4,6,20H2,(H,24,25)

105956-97-6SDS

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 7-(3-Aminopyrrolidin-1-yl)-8-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names Clinafloxacin

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:105956-97-6 SDS

105956-97-6Relevant articles and documents

Method for making quinoline carboxylic acids or naphthyridine carboxylic acids in free base form

-

, (2008/06/13)

The present invention provides a method of making quinolone carboxylic acids or naphthyridine carboxylic acids in free base form, the method comprising dissolving a quinolone carboxylic acid salt or naphthyridine carboxylic acid salt in a solvent system to form a solution; combining the solution containing the quinolone carboxylic acid salt or naphthyridine carboxylic acid salt with a calcium salt in an amount in the range of about 0.01% to about 5.0% by weight of the quinolone carboxylic acid salt or naphthyridine carboxylic acid salt and a base, the combination resulting in the formation of a precipitate; and collecting the precipitate. Also provided is a solid bulk pharmaceutical chemical composition which is the product resulting from the precipitation.

Process for the synthesis of 3-chloro-2,4,5-trifluorobenzoic acid

-

, (2008/06/13)

An improved process for the preparation of 3-chloro-2,4,5-trifluorobenzoic acid is described which involves reaction of a diester of 3,4,5,6-tetrafluoro-1,2-benzenedicarboxylic acid with a substituted amine to afford 3-amino-2,4,5-trifluorobenzoic acid followed by subsequent conversion of the amio intermediate into 3-chloro-2,4,5-trifluorobenzoic acid.

Process and intermediates for quinolonecaboxylic acid

-

, (2008/06/13)

The present invention is concerned with a certain novel process for the preparation of a quinolonecarboxylic acid of the following formula; and with intermediates of the following formula; wherein R is hydrogen atom or lower alkyl group, X is halogen atom

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