900501
Potassium carbonate
anhydrous, free-flowing, Redi-Dri™, ReagentPlus®, 99%
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A propos de cet article
Formule linéaire :
K2CO3
Numéro CAS:
Poids moléculaire :
138.21
UNSPSC Code:
12352302
NACRES:
NA.21
PubChem Substance ID:
EC Number:
209-529-3
Beilstein/REAXYS Number:
4267587
MDL number:
Assay:
99%
Grade:
anhydrous
Form:
powder
Service technique
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anhydrous
Quality Level
product line
ReagentPlus®, Redi-Dri™
assay
99%
form
powder
quality
free-flowing
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
Application
- Improved 2-pyridyl reductive homocoupling reaction using biorenewable solvent: A detailed examination of using potassium carbonate in an enhanced reductive homocoupling of 2-pyridyl compounds in a biorenewable solvent, showcasing a sustainable approach to chemical synthesis (Webb et al., 2023).
- Fe(3)O(4)@void@C-Schiff-base/Pd yolk-shell nanostructures as a nanocatalyst for Suzuki coupling reaction: Discusses the development of a palladium-based nanocatalyst supported by potassium carbonate for improved Suzuki coupling reactions, an important reaction in organic chemistry (Barzkar et al., 2023).
- Enhanced LC-ESI-MS/MS Sensitivity by Cationic Derivatization of Organophosphorus Acids: Study on enhancing liquid chromatography-electrospray ionization tandem mass spectrometry sensitivity using potassium carbonate, improving the detection of organophosphorus acids (Shamai Yamin et al., 2023).
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Classe de stockage
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Heck reaction using palladium complexed to dendrimers on silica.
Alper H, et al.
Canadian Journal of Chemistry, 78(6), 920-924 (2000)
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.