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Merck
CN

925918

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

95%, powder

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关于此项目

经验公式(希尔记法):
C28H24BrNO
化学文摘社编号:
分子量:
470.40
MDL number:
UNSPSC Code:
12352101
NACRES:
NA.21
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产品名称

9-(2,6-Dimethylphenyl)-1-methoxy-10-phenylacridinium bromide, 95%

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

assay

95%

form

powder

reaction suitability

reagent type: catalyst
reaction type: Cross Couplings

mp

190-198 (decomp)

Quality Level

Legal Information

Product of Solvias

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)

存储类别

11 - Combustible Solids

wgk

WGK 3

法规信息

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分析证书(COA)

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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
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

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