Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.1745 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COCC(=O)C1=CC=CC=C1
InChI
InChIKey=YRNDGUSDBCARGC-UHFFFAOYSA-N
InChI=1S/C9H10O2/c1-11-7-9(10)8-5-3-2-4-6-8/h2-6H,7H2,1H3
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.1745 |
| 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 |
|---|---|---|
| Didymosphaeria igniaria: a new microorganism useful for the enantioselective reduction of aryl-aliphatic ketones. | 2010-11 |
|
| (1E,2E)-1,2-Bis[1-(2-methoxy-phen-yl)ethyl-idene]hydrazine. | 2010-10-31 |
|
| Aerobic oxidation of lignin models using a base metal vanadium catalyst. | 2010-06-21 |
|
| Neurochemical approaches in the laboratory diagnosis of Parkinson and Parkinson dementia syndromes: a review. | 2009 |
|
| Use of an ex vivo local lymph node assay to assess contact hypersensitivity potential. | 2008-07 |
|
| Dynamic liquid phase nanoextraction coupled to GC/MS for rapid analysis of methoxyacetophenone and anisaldehyde isomers in urine. | 2008-07 |
|
| Synthesis and physiological activity of thiophenes and furans with 3- and 4-methoxyacetophenone derivatives. | 2008 |
|
| Role of guiding groups in cinchona-modified platinum for controlling the sense of enantiodifferentiation in the hydrogenation of ketones. | 2007-08-29 |
|
| Combining drop-to-drop solvent microextraction with gas chromatography/mass spectrometry using electronic ionization and self-ion/molecule reaction method to determine methoxyacetophenone isomers in one drop of water. | 2006-03-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 14:55:27 GMT 2025
by
admin
on
Wed Apr 02 14:55:27 GMT 2025
|
| Record UNII |
Y4V7A57H8F
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
4079-52-1
Created by
admin on Wed Apr 02 14:55:27 GMT 2025 , Edited by admin on Wed Apr 02 14:55:27 GMT 2025
|
PRIMARY | |||
|
354
Created by
admin on Wed Apr 02 14:55:27 GMT 2025 , Edited by admin on Wed Apr 02 14:55:27 GMT 2025
|
PRIMARY | |||
|
DTXSID90193778
Created by
admin on Wed Apr 02 14:55:27 GMT 2025 , Edited by admin on Wed Apr 02 14:55:27 GMT 2025
|
PRIMARY | |||
|
77698
Created by
admin on Wed Apr 02 14:55:27 GMT 2025 , Edited by admin on Wed Apr 02 14:55:27 GMT 2025
|
PRIMARY | |||
|
227212
Created by
admin on Wed Apr 02 14:55:27 GMT 2025 , Edited by admin on Wed Apr 02 14:55:27 GMT 2025
|
PRIMARY | |||
|
52400
Created by
admin on Wed Apr 02 14:55:27 GMT 2025 , Edited by admin on Wed Apr 02 14:55:27 GMT 2025
|
PRIMARY | |||
|
223-802-4
Created by
admin on Wed Apr 02 14:55:27 GMT 2025 , Edited by admin on Wed Apr 02 14:55:27 GMT 2025
|
PRIMARY | |||
|
Y4V7A57H8F
Created by
admin on Wed Apr 02 14:55:27 GMT 2025 , Edited by admin on Wed Apr 02 14:55:27 GMT 2025
|
PRIMARY |