907502
Potassium 5-bromo-1H-indole-1-carbodithioate
≥95%
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About This Item
Empirical Formula (Hill Notation):
C9H5BrKNS2
Molecular Weight:
310.28
UNSPSC Code:
12352101
NACRES:
NA.22
Recommended Products
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)
related product
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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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
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