Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H13NO |
| Molecular Weight | 223.2698 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=CC=C2CC3=CC=CC=C3C2=C1
InChI
InChIKey=WIGMLEPKVNVQSQ-UHFFFAOYSA-N
InChI=1S/C15H13NO/c1-10(17)16-13-7-6-12-8-11-4-2-3-5-14(11)15(12)9-13/h2-7,9H,8H2,1H3,(H,16,17)
| Molecular Formula | C15H13NO |
| Molecular Weight | 223.2698 |
| 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 |
|---|---|---|
| Chromosomal localization of a unique gene by non-autoradiographic in situ hybridization. | 1985-09-12 |
|
| Effect of the structural isomer N-3-fluorenylacetamide on microsomal binding and hydroxylation of the carcinogen N-2-fluorenylacetamide. | 1981-06-01 |
|
| New 9-stubstituted 3-N,O-diacetylhydroxylaminofluorenes: enhanced electrophilicity and mutagenicity. Derivatives of fluorene. 38. | 1980-03 |
|
| Sensitivity of the conformation of deoxyguanosine to binding at the C-8 position by N-acetylated and unacetylated 2-aminofluorene. | 1980 |
|
| Microsomal metabolism of arylamides by the rat and guinea pig--I. Oxidation of N-3-fluorenylacetamide at carbon-atom-9--a major metabolic reaction. | 1978 |
|
| Separation and identification of metabolites of the arylamide, N-3-fluorenyl-acetamide, by high-pressure liquid chromatography. | 1977-11-21 |
|
| Mammary carcinogenesis in the rat by topical application of fluorenylhydroxamic acids and their acetates. | 1977-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:53:01 GMT 2025
by
admin
on
Mon Mar 31 18:53:01 GMT 2025
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| Record UNII |
4P9MD74D4T
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| Record Status |
Validated (UNII)
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| Record Version |
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22722
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DTXSID40212125
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9865
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C100047
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4P9MD74D4T
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6292-55-3
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