추천 제품
Grade
reagent grade
Quality Level
vapor pressure
1 mmHg ( 220 °C)
분석
≥98%
양식
solid
환경친화적 대안 제품 특성
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
mp
256-258 °C (dec.) (lit.)
환경친화적 대안 카테고리
SMILES string
[K+].CC(C)(C)[O-]
InChI
1S/C4H9O.K/c1-4(2,3)5;/h1-3H3;/q-1;+1
InChI key
LPNYRYFBWFDTMA-UHFFFAOYSA-N
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일반 설명
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Find details here.
애플리케이션
Potassium tert-butoxide has been used as a strong base in the enantioselective synthesis of amines by transfer hydrogenation of N-(tertbutylsulfinyl)imines.
It can also be used:
It can also be used:
- To synthesize aliphatic and aromatic amides from corresponding esters and amines.
- As a base in the intramolecular cyclization of aryl ethers, amines, and amides.
- As a catalyst to prepare styrene derivatives from aryl halides and alkenes by Mizoroki-Heck reaction.
Used for greener amidation of esters.
tert-Butoxide-Assisted Amidation of Esters under Green Conditions
Potassium tert-butoxide may be used as a base in the intramolecular cyclization of iodo arene to afford benzopyran via microwave method of synthesis.
tert-Butoxide-Assisted Amidation of Esters under Green Conditions
Potassium tert-butoxide may be used as a base in the intramolecular cyclization of iodo arene to afford benzopyran via microwave method of synthesis.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Dam. 1 - Flam. Sol. 1 - Self-heat. 2 - Skin Corr. 1A
보충제 위험성
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
"Potassium tert-Butoxide Promoted Intramolecular Arylation via a Radical Pathway"
Organic Letters, 13(12), 3242-3245 (2011)
tert-Butoxide-assisted amidation of esters under green conditions
Synthesis, 44(01), 42-50 (2012)
Mizoroki-Heck-type reaction mediated by potassium tert-butoxide
Angewandte Chemie (International ed. in English), 123(20), 4767-4770 (2011)
Synthesis of highly enantiomerically enriched amines by asymmetric transfer hydrogenation of N-(tert-butylsulfinyl) imines
Organic Syntheses (2013)
Bioresource technology, 114, 1-5 (2012-04-03)
The effects of solvents with different log P values, and of lipases on the synthesis of water-soluble plant stanol derivatives were investigated. Results showed that conversion in solvents with log P<0.37 was mainly controlled by the hydrophobicity of the solvent
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