Cart (0)
No products in the cart.
Purchase CAS:2416056-30-7 | (2,2-difluorocyclopropyl)-trifluoro-boranuide,view related peer-reviewed papers,technical documents,similar products,MSDS & more.Potassium (2,2-difluorocyclopropyl)trifluoroborate, also known as potassium [2-(2,2-difluorocyclopropyl)ethyl]trifluoroboranuide, is a chemical compound with the molecular weight of 212.01 . The IUPAC name for this compound is potassium (2-(2,2-difluorocyclopropyl)ethyl)trifluoroborate . It is a pow...
Potassium (2,2-difluorocyclopropyl)trifluoroborate, also known as potassium [2-(2,2-difluorocyclopropyl)ethyl]trifluoroboranuide, is a chemical compound with the molecular weight of 212.01. The IUPAC name for this compound is potassium (2-(2,2-difluorocyclopropyl)ethyl)trifluoroborate. It is a powder that is stored at a temperature of 4 degrees Celsius.
The InChI code for Potassium (2,2-difluorocyclopropyl)trifluoroborate is 1S/C5H7BF5.K/c7-5(8)3-4(5)1-2-6(9,10)11;/h4H,1-3H2;/q-1;+1. This code provides a specific string of characters that represents the molecular structure of the compound.
Potassium (2,2-difluorocyclopropyl)trifluoroborate is a solid substance. It is stored in an inert atmosphere at temperatures between 2-8 degrees Celsius.
Potassium trifluoro(organo)borates, a group that includes compounds like Potassium;(2,2-difluorocyclopropyl)-trifluoro-boranuide, are highly stable organoboron derivatives. They have gained attention as promising alternatives to other organoboron reagents due to their interesting reactivity. These salts are particularly notable for their reactions through the formation of difluoroboranes and in transmetallation reactions with transition metals. They have shown to be more reactive than boronic acids or esters in numerous reactions (Darses & Genêt, 2003).
In a study exploring the reactivity of the boron-centred nucleophile B(CN)32-, reactions with perfluorinated arenes like hexafluorobenzene resulted in the formation of KF and the K+ salts of respective borate anions. This indicates the potential of potassium trifluoro(organo)borates in borylation and nucleophilic reactions (Landmann et al., 2017).
Research in agriculture has noted the importance of potassium in soil and plant physiology. While not directly related to Potassium;(2,2-difluorocyclopropyl)-trifluoro-boranuide, this study underlines the broader relevance of potassium in agricultural applications, which could extend to various potassium compounds (Römheld & Kirkby, 2010) .
Potassium trifluoro(organo)borates have been utilized in the synthesis of alanine derivatives, where they reacted with dehydroamino esters. This showcases their applicability in synthesizing important amino acids (Navarre, Darses & Genêt, 2004) .
In analytical chemistry, potassium-based compounds have been used in microfluidic devices for the optical recognition of potassium, indicating the versatility of potassium derivatives in analytical methods (Erenas, de Orbe-Payá & Capitán-Vallvey, 2016).
The compound is labeled with the GHS07 pictogram, indicating that it can cause certain health hazards. The hazard statements associated with it are H302, H315, H319, and H335, which indicate that it is harmful if swallowed, causes skin irritation, causes serious eye irritation, and may cause respiratory irritation respectively. Precautionary measures include avoiding breathing dust/fume/gas/mist/vapors/spray and washing thoroughly after handling.
Product Name: | (2,2-difluorocyclopropyl)-trifluoro-boranuide |
Synonyms: | (2,2-difluorocyclopropyl)-trifluoro-boranuide;potassium (2,2-difluorocyclopropyl)trifluoroboranuide;Potassium (2,2-difluorocyclopropyl)trifluoroborate;Borate(1-), (2,2-difluorocyclopropyl)trifluoro-, potassium (1:1), (T-4)- |
CAS: | 2416056-30-7 |
MF: | C3H2BF5K |
MW: | 182.95 |
EINECS: | |
Product Categories: | |
Mol File: | 2416056-30-7.mol |
(2,2-difluorocyclopropyl)-trifluoro-boranuide Chemical Properties |