ALD00162
Cyclopropanesulfonyl fluoride
95%
About This Item
Productos recomendados
Quality Level
assay
95%
form
liquid
reaction suitability
reaction type: click chemistry
refractive index
n/D 1.407
density
1.310 g/L at 25 °C
SMILES string
FS(C1CC1)(=O)=O
InChI
1S/C3H5FO2S/c4-7(5,6)3-1-2-3/h3H,1-2H2
InChI key
XPOPREDCDIARJH-UHFFFAOYSA-N
Categorías relacionadas
Application
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
148.0 °F
flash_point_c
64.44 °C
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Artículos
This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.
This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.
This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.
This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.
Contenido relacionado
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