Potassium trifluoro(3-((4-methoxyphenyl) amino)-3-oxopropyl)borate

98%

Reagent Code: #91073
fingerprint
CAS Number 1704705-14-5

science Other reagents with same CAS 1704705-14-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.11 g/mol
Formula C₁₀H₁₂BF₃KNO₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This potassium trifluoroborate compound serves as a versatile organoboron reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It enables the efficient introduction of the 3-[(4-methoxyphenyl)amino]-3-oxopropyl group into aromatic systems, facilitating the construction of complex molecules for pharmaceuticals, agrochemicals, and bioactive compounds. As a stable and air-tolerant borate intermediate, it offers precise control in C-C bond formation, enhancing selectivity and yield in medicinal chemistry applications. Its role extends to advanced synthetic methodologies in research and industrial processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿41,180.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Potassium trifluoro(3-((4-methoxyphenyl) amino)-3-oxopropyl)borate
No image available

This potassium trifluoroborate compound serves as a versatile organoboron reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It enables the efficient introduction of the 3-[(4-methoxyphenyl)amino]-3-oxopropyl group into aromatic systems, facilitating the construction of complex molecules for pharmaceuticals, agrochemicals, and bioactive compounds. As a stable and air-tolerant borate intermediate, it offers precise control in C-C bond formation, enhancing selectivity an

This potassium trifluoroborate compound serves as a versatile organoboron reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It enables the efficient introduction of the 3-[(4-methoxyphenyl)amino]-3-oxopropyl group into aromatic systems, facilitating the construction of complex molecules for pharmaceuticals, agrochemicals, and bioactive compounds. As a stable and air-tolerant borate intermediate, it offers precise control in C-C bond formation, enhancing selectivity and yield in medicinal chemistry applications. Its role extends to advanced synthetic methodologies in research and industrial processes.

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...