(4-(Piperidin-1-ylsulfonyl)-2-(trifluoromethyl)phenyl)boronic acid

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Reagent Code: #227550
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CAS Number 2096339-82-9

science Other reagents with same CAS 2096339-82-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.13 g/mol
Formula C₁₂H₁₅BF₃NO₄S
badge Registry Numbers
MDL Number MFCD18783153
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of biaryl structures in drug candidates. The piperidinylsulfonyl and trifluoromethyl groups enhance binding selectivity and metabolic stability, making it valuable in optimizing lead compounds for improved potency and pharmacokinetic properties. Commonly employed in medicinal chemistry research for targeted therapies, especially in oncology and inflammatory diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,030.00
inventory 250mg
10-20 days ฿3,450.00
inventory 1g
10-20 days ฿10,070.00
inventory 5g
10-20 days ฿37,310.00

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(4-(Piperidin-1-ylsulfonyl)-2-(trifluoromethyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of biaryl structures in drug candidates. The piperidinylsulfonyl and trifluoromethyl groups enhance binding selectivity and metabolic stability, making it valuable in optimizing lead compounds for improved potency and pharmacokinetic properties. Commonly em

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of biaryl structures in drug candidates. The piperidinylsulfonyl and trifluoromethyl groups enhance binding selectivity and metabolic stability, making it valuable in optimizing lead compounds for improved potency and pharmacokinetic properties. Commonly employed in medicinal chemistry research for targeted therapies, especially in oncology and inflammatory diseases.

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