추천 제품
제품 라인
BioXtra
분석
≥99.0%
형태
powder
불순물
≤0.0005% Phosphorus (P)
≤0.1% Insoluble matter
pH
11-13 (25 °C, 138 g/L)
mp
891 °C (lit.)
solubility
H2O: 1 M, clear, colorless
음이온 미량물
chloride (Cl-): ≤0.005%
sulfate (SO42-): ≤0.02%
양이온 미량물
Al: ≤0.0005%
Ca: ≤0.001%
Cu: ≤0.0005%
Fe: ≤0.0005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.5%
Pb: ≤0.001%
Zn: ≤0.0005%
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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Potassium carbonate is an inorganic base that is used in the alkylation of phenols and 1,3-dicarbonyl compounds, as well as the generation of sulfur and phosphorus ylides. It is also used to dry organic solvents.
애플리케이션
Potassium carbonate can be used as a catalyst in the:
- Markovnikov addition reactions.
- Suzuki cross-coupling reactions.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Potassium carbonate as a green catalyst for Markovnikov addition of azoles to vinyl acetate in PEG
Green Chemistry Letters and Reviews, 6, 63-68 (2013)
Potassium Carbonate Promoted C-N Coupling Reaction between Benzamides and Aryl Iodides
Synthesis, 50, 1090-1096 (2018)
Application of experimental design and multivariate analysis in the on-line reaction monitoring of a Suzuki cross-coupling reaction by Raman spectroscopy and multivariate analysis
Vibrational Spectroscopy, 100, 93-98 (2019)
Potassium Carbonate
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
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
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