Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H8Br2 |
| Molecular Weight | 336.021 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
BrC1=C2C=CC=CC2=C(Br)C3=CC=CC=C13
InChI
InChIKey=BRUOAURMAFDGLP-UHFFFAOYSA-N
InChI=1S/C14H8Br2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H
| Molecular Formula | C14H8Br2 |
| Molecular Weight | 336.021 |
| 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 and characterization of a heteroleptic Ru(II) complex of phenanthroline containing oligo-anthracenyl carboxylic acid moieties. | 2010-09-08 |
|
| Photochemistry of far red responsive tetrahydroquinoxaline-based squaraine dyes. | 2010-03-04 |
|
| 4,4'-(Anthracene-9,10-di-yl)dibenzoic acid dimethyl-formamide disolvate. | 2009-05-07 |
|
| Structural and variable-temperature NMR studies of 9-diisopropylphosphanylanthracenes and 9,10-bis(diisopropylphosphanyl)anthracenes and their oxidation products. | 2008-07-18 |
|
| Highly brominated anthracenes as precursors for the convenient synthesis of 2,9,10-trisubstituted anthracene derivatives. | 2008 |
|
| UVA photoirradiation of halogenated-polycyclic aromatic hydrocarbons leading to induction of lipid peroxidation. | 2006-06 |
|
| One step Pd(0)-catalyzed synthesis, X-ray analysis, and photophysical properties of cyclopent[hi]aceanthrylene: fullerene-like properties in a nonalternant cyclopentafused aromatic hydrocarbon. | 2002-01-09 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:11:45 GMT 2025
by
admin
on
Mon Mar 31 21:11:45 GMT 2025
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| Record UNII |
61CP7C5Y82
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| Record Status |
Validated (UNII)
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| Record Version |
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m4293
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68226
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9,10-Dibromoanthracene
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