1023357-63-2 | Potassium 3-trifluoroboratopropionate methyl ester

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$113.00	$79.00
5g	96%	in stock	$393.00	$275.00
10g	96%	in stock	$634.00	$444.00
25g	96%	in stock	$1,209.00	$846.00

Description

• Catalog Number: AA09140
• Chemical Name: Potassium 3-trifluoroboratopropionate methyl ester
• CAS Number: 1023357-63-2
• Molecular Formula: C4H7BF3KO2
• Molecular Weight: 194.0017
• MDL Number: MFCD09992947
• SMILES: F[B-](CCC(=O)OC)(F)F.[K+]

Computed Properties

• Complexity: 127
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3

Upstream Synthesis Route

Potassium trifluoro(3-methoxy-3-oxopropyl)borate is a versatile reagent widely used in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a powerful tool in the formation of carbon-carbon and carbon-heteroatom bonds, making it a key component in the construction of complex organic molecules.One of the key applications of Potassium trifluoro(3-methoxy-3-oxopropyl)borate is in the Suzuki-Miyaura cross-coupling reaction, a fundamental method for the formation of biaryl compounds. By serving as the boron component in this reaction, Potassium trifluoro(3-methoxy-3-oxopropyl)borate facilitates the coupling of aryl halides with boronic acids or esters, leading to the synthesis of a wide range of functionalized biaryl systems.Additionally, this reagent is utilized in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals where the formation of complex carbon-carbon bonds is essential. Its unique structural features and reactivity make it a valuable tool for chemical researchers looking to streamline the synthesis of intricate organic molecules with high efficiency and selectivity.