Potassium (E)-trifluoro(prop-1-en-1-yl)borate

95%

Reagent Code: #87936
fingerprint
CAS Number 1902198-18-8

science Other reagents with same CAS 1902198-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.98 g/mol
Formula C₃H₅BF₃K
badge Registry Numbers
MDL Number MFCD09992882
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily used in organic synthesis as a reagent for the introduction of the trifluoro(prop-1-en-1-yl) group into various organic molecules. It is particularly valuable in cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the construction of complex molecular structures. The compound is often employed in the synthesis of pharmaceuticals and agrochemicals, where the trifluoro(prop-1-en-1-yl) moiety can impart desirable properties such as increased stability or enhanced biological activity. Additionally, it is utilized in materials science for the development of advanced polymers and coatings, leveraging its unique chemical properties to improve material performance.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿32,634.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Potassium (E)-trifluoro(prop-1-en-1-yl)borate
No image available
This chemical is primarily used in organic synthesis as a reagent for the introduction of the trifluoro(prop-1-en-1-yl) group into various organic molecules. It is particularly valuable in cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the construction of complex molecular structures. The compound is often employed in the synthesis of pharmaceuticals and agrochemicals, where the trifluoro(prop-1-en-1-yl) moiety can impart desirable properties such as increased
This chemical is primarily used in organic synthesis as a reagent for the introduction of the trifluoro(prop-1-en-1-yl) group into various organic molecules. It is particularly valuable in cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the construction of complex molecular structures. The compound is often employed in the synthesis of pharmaceuticals and agrochemicals, where the trifluoro(prop-1-en-1-yl) moiety can impart desirable properties such as increased stability or enhanced biological activity. Additionally, it is utilized in materials science for the development of advanced polymers and coatings, leveraging its unique chemical properties to improve material performance.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...