Details
Stereochemistry | ACHIRAL |
Molecular Formula | C17H20N2O |
Molecular Weight | 268.3535 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)N(C)C
InChI
InChIKey=VVBLNCFGVYUYGU-UHFFFAOYSA-N
InChI=1S/C17H20N2O/c1-18(2)15-9-5-13(6-10-15)17(20)14-7-11-16(12-8-14)19(3)4/h5-12H,1-4H3
Molecular Formula | C17H20N2O |
Molecular Weight | 268.3535 |
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 |
---|---|---|
Bioassay of Michler's Ketone for Possible Carcinogenicity (CAS No. 90-94-8). | 1979 |
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Hepatitis C viral IRES inhibition by phenazine and phenazine-like molecules. | 2000 Jun 5 |
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Control of hepatitis C: a medicinal chemistry perspective. | 2005 Jan 13 |
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Determination of ionic liquids solvent properties using an unusual probe: the electron donor-acceptor complex between 4,4'-bis(dimethylamino)-benzophenone and tetracyanoethene. | 2006 Apr 13 |
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Mechanistic studies of the photocatalytic degradation of methyl green: an investigation of products of the decomposition processes. | 2007 Jun 15 |
|
Electrochemical degradation of crystal violet with BDD electrodes: effect of electrochemical parameters and identification of organic by-products. | 2010 Sep |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:08:56 GMT 2023
by
admin
on
Fri Dec 15 17:08:56 GMT 2023
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Record UNII |
3Z2SN6B347
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C45175
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admin on Fri Dec 15 17:08:56 GMT 2023 , Edited by admin on Fri Dec 15 17:08:56 GMT 2023
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Code System | Code | Type | Description | ||
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3Z2SN6B347
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DTXSID2020894
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7031
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9602
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C44403
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C014682
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Michler's ketone
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2865
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90-94-8
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m7526
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admin on Fri Dec 15 17:08:56 GMT 2023 , Edited by admin on Fri Dec 15 17:08:56 GMT 2023
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PRIMARY | Merck Index | ||
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202-027-5
Created by
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PRIMARY |