Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H12O2 |
| Molecular Weight | 212.2439 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)C(=O)C2=CC=CC=C2
InChI
InChIKey=SWFHGTMLYIBPPA-UHFFFAOYSA-N
InChI=1S/C14H12O2/c1-16-13-9-7-12(8-10-13)14(15)11-5-3-2-4-6-11/h2-10H,1H3
| Molecular Formula | C14H12O2 |
| Molecular Weight | 212.2439 |
| 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 |
|---|---|---|
| Experimental and theoretical studies on the mechanism of photochemical hydrogen transfer from 2-aminobenzimidazole to nπ* and ππ* aromatic ketones. | 2010-09-16 |
|
| 3-(4-Methoxy-phen-yl)-1-(2-nitrophen-yl)prop-2-en-1-one. | 2009-11-18 |
|
| Coenzyme Q0 induces apoptosis and modulates the cell cycle in estrogen receptor negative breast cancer cells. | 2009-01 |
|
| The benzophenone S1(n,pi*) --> T1(n,pi*) states intersystem crossing reinvestigated by ultrafast absorption spectroscopy and multivariate curve resolution. | 2008-01-17 |
|
| Oxygen acidity of ring methoxylated 1,1-diarylalkanol radical cations bearing alpha-cyclopropyl groups. The competition between O-neophyl shift and C-cyclopropyl beta-scission in the intermediate 1,1-diarylalkoxyl radicals. | 2006-04-14 |
|
| Inversion of 4-methoxybenzophenone triplet in aqueous solutions. | 2002-09 |
|
| Severe contact urticaria and anaphylaxis from benzophenone-3(2-hydroxy 4-methoxy benzophenone). | 2002-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:04:23 GMT 2025
by
admin
on
Mon Mar 31 20:04:23 GMT 2025
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| Record UNII |
I4XJ07373M
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| Record Status |
Validated (UNII)
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