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925918

Sigma-Aldrich

9-(2,6-Dimethylphenyl)-1-methoxy-10-phenylacridinium bromide

95%

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100 MG
MXP 4,552.00

MXP 4,552.00

Estimated to ship onApril 12, 2025

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100 MG
MXP 4,552.00

About This Item

Empirical Formula (Hill Notation):
C28H24BrNO
CAS Number:
2304661-66-1
Molecular Weight:
470.40
MDL number:
MFCD34622481
UNSPSC Code:
12352101
NACRES:
NA.21

MXP 4,552.00

Estimated to ship onApril 12, 2025

Request a Bulk Order

Quality Level

100

Assay

95%

form

powder

reaction suitability

reagent type: catalyst
reaction type: Cross Couplings

mp

190-198 (decomp)

SMILES string

COC1=CC=CC2=[N+](C3=CC=CC=C3)C4=CC=CC=C4C(C5=C(C)C=CC=C5C)=C21.[Br-]

InChI

1S/C28H24NO.BrH/c1-19-11-9-12-20(2)26(19)27-22-15-7-8-16-23(22)29(21-13-5-4-6-14-21)24-17-10-18-25(30-3)28(24)27;/h4-18H,1-3H3;1H/q+1;/p-1

InChI key

AIMWDQBPPADYLB-UHFFFAOYSA-M

Application

9-(2,6-Dimethylphenyl)-1-methoxy-10-phenylacridinium bromide is an acridinium photocatalyst used for a variety of transformations.

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

Other Notes

Modulation of Acridinium Organophotoredox Catalysts Guided by Photophysical Studies

Design and application of aminoacridinium organophotoredox catalysts

Direct Transformation of Esters into Heterocyclic Fluorophores

Legal Information

Product of Solvias

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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Bouthayna Zilate et al.
Chemical communications (Cambridge, England), 56(12), 1767-1775 (2020-01-31)
Recent developments in preparative photocatalysis have reshaped synthetic strategies and now represent an integral part of current organic chemistry. Due to their favourable electrochemical and photophysical properties, the nowadays most frequently used photocatalysts are based on precious Ru- and Ir-polypyridyl
Christian Fischer et al.
Angewandte Chemie (International ed. in English), 57(9), 2436-2440 (2017-12-19)
Despite the manifold use of heterocyclic fluorophores, only a fraction of the desired dye diversity can be accessed by contemporary synthetic approaches. Herein, we describe a modular method that converts various carboxylic acid esters directly into a broad spectrum of

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