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About This Item
Empirical Formula (Hill Notation):
C44H24ClN5
CAS Number:
Molecular Weight:
658.15
MDL number:
UNSPSC Code:
12352101
NACRES:
NA.22
Form:
powder or crystals
Product Name
3CzClIPN,
form
powder or crystals
reaction suitability
reagent type: catalyst, core: carbazole
reaction type: Photocatalysis
mp
>300 °C
SMILES string
Clc1c(c(c(c(c1[n]8c9c(c%10c8cccc%10)cccc9)C#N)[n]5c6c(c7c5cccc7)cccc6)C#N)[n]2c3c(c4c2cccc4)cccc3
InChI
1S/C44H24ClN5/c45-41-43(49-37-21-9-3-15-29(37)30-16-4-10-22-38(30)49)33(25-46)42(48-35-19-7-1-13-27(35)28-14-2-8-20-36(28)48)34(26-47)44(41)50-39-23-11-5-17-31(39)32-18-6-12-24-40(32)50/h1-24H
InChI key
AETFKBFYWGEUOV-UHFFFAOYSA-N
Application
3CzClIPN is cyanoarene-based donor-acceptor photocatalyst developed by the Zeitler group. While this catalyst has a balanced redox profile, allowing for its use in a variety of transformations, it stands out as the most oxidizing catalyst of the family.
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)
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Elisabeth Speckmeier et al.
Journal of the American Chemical Society, 140(45), 15353-15365 (2018-10-03)
The targeted choice of specific photocatalysts has been shown to play a critical role for the successful realization of challenging photoredox catalytic transformations. Herein, we demonstrate the successful implementation of a rational design strategy for a series of deliberate structural