Details
Stereochemistry | ACHIRAL |
Molecular Formula | C8H6Cl2O |
Molecular Weight | 189.039 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C1=C(Cl)C=C(Cl)C=C1
InChI
InChIKey=XMCRWEBERCXJCH-UHFFFAOYSA-N
InChI=1S/C8H6Cl2O/c1-5(11)7-3-2-6(9)4-8(7)10/h2-4H,1H3
Molecular Formula | C8H6Cl2O |
Molecular Weight | 189.039 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Synthesis and antibacterial activity of some novel N-substituted piperazinyl-quinolones. | 2001 Nov-Dec |
|
[Synthesis of a new cyclodextrin derivative and its application as CGC chiral stationary phase in determination of enantiomeric excess]. | 2002 Jan |
|
Antituberculosis agents. VII. Synthesis and in vitro evaluation of antimycobacterial activity and cytotoxicity of some N-piperazinyl quinolone derivatives. | 2003 Apr |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 06:04:26 GMT 2023
by
admin
on
Sat Dec 16 06:04:26 GMT 2023
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Record UNII |
T7F2608H5H
|
Record Status |
Validated (UNII)
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Record Version |
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33945
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218-780-8
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DTXSID1022182
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2234-16-4
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C036847
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T7F2608H5H
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16693
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admin on Sat Dec 16 06:04:26 GMT 2023 , Edited by admin on Sat Dec 16 06:04:26 GMT 2023
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