156671
Potassium tert-butoxide
reagent grade, ≥98%
Synonym(s):
Potassium tert-butylate, Potassium t-butoxide
About This Item
Recommended Products
grade
reagent grade
Quality Level
vapor pressure
1 mmHg ( 220 °C)
Assay
≥98%
form
solid
greener alternative product characteristics
Catalysis
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sustainability
Greener Alternative Product
mp
256-258 °C (dec.) (lit.)
greener alternative category
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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General description
Application
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.
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Flam. Sol. 1 - Self-heat. 2 - Skin Corr. 1A
Supplementary Hazards
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Protocols
Information on the Amide bond and the Catalytic Amide Bond Formation Protocol. Amidation of amines and alcohols. The amide bond, an important linkage in organic chemistry, is a key functional group in peptides, polymers, and many natural products and pharmaceuticals.
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