Produktname:(10-(Naphthalen-1-yl)anthracen-9-yl)boronic acid
IUPAC Name:[10-(naphthalen-1-yl)anthracen-9-yl]boronic acid
- CAS:400607-46-7
- Molekulare Formel:C24H17BO2
- Reinheit:98%
- Katalognummer:CM135304
- Molekulargewicht:348.20
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Produkt-Details
- CAS-Nr.:400607-46-7
- Molekulare Formel:C24H17BO2
- Schmelzpunkt:-
- SMILES-Code:OB(C1=C2C=CC=CC2=C(C3=C4C=CC=CC4=CC=C3)C5=CC=CC=C15)O
- Dichte:
- Katalognummer:CM135304
- Molekulargewicht:348.20
- Siedepunkt:574.2°C at 760 mmHg
- Mdl-Nr.:MFCD11977302
- Lagerung:
Category Infos
- Anthracenes
- Anthracene is a condensed aromatic hydrocarbon containing three rings. The center of the three rings of anthracene is in a straight line, which is the isomer of phenanthrene. The chemical activity of the 9 and 10 positions in the anthracene molecule is relatively high. It is oxidized with nitric acid to generate 9, 10-anthraquinone, which is an important intermediate for the synthesis of anthraquinone dyes. Anthracene can also act as a conjugated diene in a Diels-Alder reaction with maleic anhydride.
Column Infos
- Boronic Acids and Esters
- Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).