(3-(Trifluoromethyl)pyridin-4-yl)boronic acid

95%

Reagent Code: #131447
fingerprint
CAS Number 1204334-17-7

science Other reagents with same CAS 1204334-17-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.92 g/mol
Formula C₆H₅BF₃NO₂
badge Registry Numbers
MDL Number MFCD11975905
thermostat Physical Properties
Boiling Point 307.0±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.44±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of bioactive molecules and drug candidates. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in the development of complex organic structures. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds, which are prevalent in kinase inhibitors and other therapeutic agents. Also utilized in agrochemical research for designing novel active ingredients with improved metabolic stability and binding affinity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿13,110.00
250mg
10-20 days ฿27,530.00
(3-(Trifluoromethyl)pyridin-4-yl)boronic acid
No image available

Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of bioactive molecules and drug candidates. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in the development of complex organic structures. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds, which are prevalent in kinase inhibitors and other therapeutic agents. Also utilized in agroc

Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of bioactive molecules and drug candidates. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds in the development of complex organic structures. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds, which are prevalent in kinase inhibitors and other therapeutic agents. Also utilized in agrochemical research for designing novel active ingredients with improved metabolic stability and binding affinity.

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...