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この商品について
化学式:
K2CO3
CAS番号:
分子量:
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:
anhydrous, reagent grade
Form:
powder
InChI key
BWHMMNNQKKPAPP-UHFFFAOYSA-L
InChI
1S/CH2O3.2K/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
SMILES string
[K+].[K+].[O-]C([O-])=O
grade
anhydrous, reagent grade
product line
Redi-Dri™
assay
≥98%
form
powder
quality
free-flowing
particle size
−325 mesh
pH
11-13 (25 °C, 138 g/L)
mp
891 °C (lit.)
Quality Level
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関連するカテゴリー
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.
Legal Information
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
保管分類
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
名称等を表示すべき危険物及び有害物
ishl_indicated
名称等を通知すべき危険物及び有害物
ishl_notified
900502-12KG: + 900502-1KG: + 900502-BULK: + 900502-2.5KG: + 900502-500G:
jan
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.
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)
Chelating N-heterocyclic carbene ligands in palladium-catalyzed Heck-type reactions.
Herrmann WA, et al.
Journal of Organometallic Chemistry, 557(1), 93-96 (1998)
Heck reaction using palladium complexed to dendrimers on silica.
Alper H, et al.
Canadian Journal of Chemistry, 78(6), 920-924 (2000)
Carlos Arroniz et al.
Organic letters, 15(4), 910-913 (2013-02-05)
ortho-Arylation of ortho-substituted benzoic acids is a challenging process due to the tendency of the reaction products toward Pd-catalyzed protodecarboxylation. A simple method for preventing decarboxylation in sterically hindered benzoic acids is reported. The method described represents a reliable and
資料
Redi-Dri™ prevents hygroscopic powders, such as inorganic salts, from absorbing moisture and forming clumps, leaving the salts free-flowing every time.
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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