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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
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)
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
新产品
此项目有
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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