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About This Item
Empirical Formula (Hill Notation):
C9H5BrKNS2
Molecular Weight:
310.28
UNSPSC Code:
12352101
NACRES:
NA.22
Product Name
Potassium 5-bromo-1H-indole-1-carbodithioate, ≥95%
assay
≥95%
form
powder or crystals
reaction suitability
reaction type: Photocatalysis, reagent type: catalyst
mp
179-185 °C
storage temp.
2-8°C
Application
Potassium 5-bromo-1H-indole-1-carbodithioate is an organic photocatalyst shown to activate alkyl electrophiles via an SN2 pathway.
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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Photochemical generation of radicals from alkyl electrophiles using a nucleophilic organic catalyst.
Bertrand Schweitzer-Chaput et al.
Nature chemistry, 11(2), 129-135 (2018-12-05)
Chemists extensively use free radical reactivity for applications in organic synthesis, materials science, and life science. Traditionally, generating radicals requires strategies that exploit the bond dissociation energy or the redox properties of the precursors. Here, we disclose a photochemical catalytic
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 907502-100MG | 04022536047041 |
| 907502-250MG | 04022536047089 |