Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.1626 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=CC=C1C(N)=O
InChI
InChIKey=MNWSGMTUGXNYHJ-UHFFFAOYSA-N
InChI=1S/C8H9NO2/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3,(H2,9,10)
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.1626 |
| 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 |
|---|---|---|
| Thiourea-catalyzed asymmetric michael addition of activated methylene compounds to alpha,beta-unsaturated imides: dual activation of imide by intra- and intermolecular hydrogen bonding. | 2006 Jul 26 |
|
| Structural considerations for designing adenosine analogs as selective inhibitors of Trichomonas sp. glyceraldehyde-3- phosphate dehydrogenase. | 2007 |
|
| Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases). | 2009 Mar |
|
| QSAR prediction of D2 receptor antagonistic activity of 6-methoxy benzamides. | 2010 Nov |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 07:55:45 GMT 2023
by
admin
on
Sat Dec 16 07:55:45 GMT 2023
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| Record UNII |
WRY8DDN8YC
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| Record Status |
Validated (UNII)
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| Record Version |
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84232
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DTXSID6022189
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