| Weight | 332.406 g/mol |
|---|---|
| Formula | C24H16N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 5 |
| Rotatable Bonds | 2 |
Bathophenanthroline (1662-01-7, 68309-97-7)
Score:
#1592 in Physics
,
#1750 in Biochemistry
,
#4858 in Chemistry
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- A comparison between Sypro Ruby and ruthenium II tris (bathophenanthroline disulfonate) as fluorescent stains for protein detection in gels. (Proteomics, 2001)
- High electron mobility in bathophenanthroline (Applied Physics Letters, 2000)
- An improved formulation of SYPRO Ruby protein gel stain: Comparison with the original formulation and with a ruthenium II tris (bathophenanthroline disulfonate) formulation (Proteomics, 2002)
- Bathophenanthrolineruthenium(II) complexes as nonradioactive labels for oligonucleotides which can be measured by timeresolved fluorescence techniques (Helvetica Chimica Acta, 1988)
- Novel Bipolar Bathophenanthroline Containing Hosts for Highly Efficient Phosphorescent OLEDs (Organic Letters, 2008)
- Determination of Ferrous Iron in the Presence of Ferric Iron with Bathophenanthroline (PDF) (Journal American Water Works Association, 1960)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C2=C3C=CC4=C(C=CN=C4C3=NC=C2)C5=CC=CC=C5
-
InChIKeyDHDHJYNTEFLIHY-UHFFFAOYSA-N
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Synthesis
Phenylboronic acid
+
Reactant
(Suzuki)
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Bathophenanthroline
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