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About This Item
Linear Formula:
K2CO3
CAS Number:
Molecular Weight:
138.21
UNSPSC Code:
12352302
NACRES:
NA.21
PubChem Substance ID:
EC Number:
209-529-3
Beilstein/REAXYS Number:
4267587
MDL number:
Assay:
≥98%
Grade:
reagent grade
Form:
powder
grade
reagent grade
Quality Level
assay
≥98%
form
powder
particle size
−325 mesh
pH
11-13 (25 °C, 138 g/L)
mp
891 °C (lit.)
SMILES string
[K+].[K+].[O-]C([O-])=O
InChI
1S/CH2O3.2K/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
InChI key
BWHMMNNQKKPAPP-UHFFFAOYSA-L
General description
Potassium carbonate is an inorganic base. It participates as base in the palladacycle catalyzed Heck reaction of chlorobenzene with styrene.
Application
Potassium carbonate was used in the following studies:
- Synthesis of polysubstituted iodobenzene derivatives.
- As base for the synthesis of high molecular weight homopolymers and copolymers derived from various bisphenols.
- As base for the Suzuki coupling of aryl halides with aryl boronic acids.
- As base for the Heck reaction of styrene and bromobenzene.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Synthesis, kinetic observations and characteristics of polyarylene ether sulphones prepared via a potassium carbonate DMAC process.
Viswanathan R, et al.
Polymer, 25(12), 1827-1836 (1984)
Robert Möckel et al.
Organic letters, 17(7), 1644-1647 (2015-03-21)
The cobalt-catalyzed Diels-Alder reaction of trimethylsilyl-substituted alkynes with 1,3-dienes led to dihydroaromatic intermediates which were transformed into iodobenzene derivatives. For this transformation, the dihydroaromatic intermediates had to be oxidized and the trimethylsilyl-substituted arene had to undergo a silicon-iodine exchange reaction.
Chelating N-heterocyclic carbene ligands in palladium-catalyzed Heck-type reactions.
Herrmann WA, et al.
Journal of Organometallic Chemistry, 557(1), 93-96 (1998)
