Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H9NO |
| Molecular Weight | 135.1632 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C1=C(N)C=CC=C1
InChI
InChIKey=GTDQGKWDWVUKTI-UHFFFAOYSA-N
InChI=1S/C8H9NO/c1-6(10)7-4-2-3-5-8(7)9/h2-5H,9H2,1H3
| Molecular Formula | C8H9NO |
| Molecular Weight | 135.1632 |
| 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 |
|---|---|---|
| Evaluation of sample recovery of malodorous livestock gases from air sampling bags, solid-phase microextraction fibers, Tenax TA sorbent tubes, and sampling canisters. | 2005 Aug |
|
| An advantageous route to oxcarbazepine (trileptal) based on palladium-catalyzed arylations free of transmetallating agents. | 2005 Oct 27 |
|
| 3-(2-Acetyl-anilino)propanoic acid. | 2008 Nov 13 |
|
| N-(2-Acetyl-phen-yl)benzene-sulfonamide. | 2009 Aug 26 |
|
| Glycosylation of aromatic amines III: Mechanistic implications of the pH-dependent glycosylation of various aromatic amines (kynurenine, 2'-aminoacetophenone, daptomycin, and sulfamethoxzaole). | 2009 Dec |
|
| Zinc-catalyzed reactions of ethenetricarboxylates with 2-(trimethylsilylethynyl)anilines leading to bridged quinoline derivatives. | 2009 Jul 2 |
|
| N-[2-(4-Methyl-2-quinol-yl)phen-yl]acetamide: a P1 structure with Z = 4. | 2010 Jul 17 |
|
| (E)-N-{2-[1-(Benzyl-imino)eth-yl]phen-yl}benzamide. | 2010 Mar 3 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:32:01 GMT 2023
by
admin
on
Fri Dec 15 18:32:01 GMT 2023
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| Record UNII |
69Y77091BC
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| Record Status |
Validated (UNII)
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| Record Version |
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