Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C26H22O2 |
| Molecular Weight | 366.4517 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(C1=CC=CC=C1)(C2=CC=CC=C2)C(O)(C3=CC=CC=C3)C4=CC=CC=C4
InChI
InChIKey=MFEWNFVBWPABCX-UHFFFAOYSA-N
InChI=1S/C26H22O2/c27-25(21-13-5-1-6-14-21,22-15-7-2-8-16-22)26(28,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20,27-28H
| Molecular Formula | C26H22O2 |
| Molecular Weight | 366.4517 |
| 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 |
|---|---|---|
| Synthesis, spectroscopy and photochemistry of novel branched fluorescent nitro-stilbene derivatives with benzopheonone groups. | 2010-05 |
|
| Synthesis of alpha-trifluoromethyl alpha-amino acids with aromatic, heteroaromatic and ferrocenyl subunits in the side chain. | 2006-07 |
|
| BF3.2CF3CH2OH (BF3.2TFE), an efficient superacidic catalyst for some organic synthetic transformations. | 2006-05-12 |
|
| Reduction of benzophenone by SmI2: the role of proton donors in determining product distribution. | 2005-09-15 |
|
| Synthesis, structure, and reactions of (acylimino)triaryl-lambda(5)-bismuthanes: first comparative study of the (acylimino)pnictorane series. | 2001-11-07 |
|
| Diverse heteroleptic ytterbium(III) thiocyanate complexes by oxidation from bis(thiocyanato)ytterbium(II). | 2001-04-17 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:36:34 GMT 2025
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admin
on
Mon Mar 31 20:36:34 GMT 2025
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4VNT36L0QZ
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