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108138-17-6

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108138-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108138-17-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,3 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108138-17:
(8*1)+(7*0)+(6*8)+(5*1)+(4*3)+(3*8)+(2*1)+(1*7)=106
106 % 10 = 6
So 108138-17-6 is a valid CAS Registry Number.

108138-17-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-difluoro-1-(2,4-difluorophenyl)-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names .ethyl 1-(2,4-difluorophenyl)-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate

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:108138-17-6 SDS

108138-17-6Downstream Products

108138-17-6Relevant articles and documents

PROCESSES FOR PREPARING QUINOLONECARBOXYLATE DERIVATIVES

-

Page 7-8, (2008/06/13)

The present invention provides a process for preparing quinolonecarboxylate derivatives under a mild condition in high yield, so as to be favorably applied to a large-scale mass production thereof.

Synthesis, Antibacterial Activities, and Pharmacological Properties of Enantiomers of Temafloxacin Hydrochloride

Chu, Daniel T. W.,Nordeen, Carl W.,Hardy, Dwight J.,Swanson, Robert N.,Giardina, William J.,et al.

, p. 168 - 174 (2007/10/02)

Temafloxacin hydrochloride is a potent member of the 4-pyridone-3-carboxylic acid class of antibacterial agents and is currently under clinical development as a broad-spectrum antimicrobial agent.It is a racemate having a chiral center at the C3 of the 7-piperazin-1-yl group.The two enantiomers were synthesized and tested for their antibacterial activities.Although no difference in in vitro antibacterial activities was observed, a minor difference in in vivo antibacterial activities was observed.However, they both exhibited similar pharmacological profiles.

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