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形狀
liquid
品質等級
反應適用性
core: potassium
濃度
1.0 M in THF
密度
0.902 g/mL at 25 °C
SMILES 字串
[K+].CC(C)(C)[O-]
InChI
1S/C4H9O.K/c1-4(2,3)5;/h1-3H3;/q-1;+1
InChI 密鑰
LPNYRYFBWFDTMA-UHFFFAOYSA-N
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一般說明
叔丁醇钾溶液是一种强非亲核碱。它能够使碳和其他布朗斯台德酸去质子化。叔丁醇中的试剂溶液可以通过使无水醇与钾在氮气氛中反应来制备。
應用
叔丁二氧化钾溶液(t-BuOK)可用于:
- 作为菜籽油与乙酸甲酯酯化反应的催化剂。
- 在温和条件下促进N-苯基氨基酸衍生的酰化铵的 Sommelet-Hauser 重排反应。
- 作为化学气相沉积法合成 KNbO3 铁电薄膜的金属有机前驱体。
- 制备 3-钾肟基吡啶催化剂。
- 作为强醇基试剂。
訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
標靶器官
Central nervous system, Respiratory system
安全危害
儲存類別代碼
4.3 - Hazardous materials which set free flammable gases upon contact with water
水污染物質分類(WGK)
WGK 1
閃點(°F)
-2.2 °F - closed cup
閃點(°C)
-19 °C - closed cup
其他客户在看
One-step methodology for the synthesis of FA picolinyl esters from intact lipids.
Journal of the American Oil Chemists' Society, 79(3), 253-256 (2002)
Chemical communications (Cambridge, England), 48(64), 8006-8008 (2012-07-10)
The regio- and diastereoselective silaboration of aromatic alkenes with a silylboron compound proceeds in the presence of a catalytic amount of potassium tert-butoxide, providing a complementary method to the corresponding transition metal-catalyzed reactions.
The Journal of organic chemistry, 74(3), 1124-1129 (2008-12-24)
3-Aryltetronic acids were prepared in one step by treatment of a mixture of methyl arylacetates and methyl hydroxyacetates with potassium tert-butoxide, via tandem transesterification/Dieckmann condensation. Several mushroom or lichen pigments, vulpinic acids, were synthesized from 3-(4-methoxyphenyl)tetronic acid in three steps
Chemistry (Weinheim an der Bergstrasse, Germany), 12(19), 4954-4963 (2006-05-04)
This paper chronicles the conceptual development, proof of principle experiments, and recent advances in the palladium-catalyzed cross-coupling reactions of the conjugate bases of organosilanols. The discovery that led to the design and refinement of this process represents a classical illustration
Organic letters, 14(17), 4466-4469 (2012-08-16)
A transition-metal-free intramolecular dehydrohalide coupling via intramolecular homolytic aromatic substitution (HAS) with aryl radicals has been developed in the presence of potassium tert-butoxide and an organic molecule as the catalyst. The methodology has been applied to a concise synthesis of
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