2-(METHYLTHIO)PYRIMIDINE-5-BORONIC ACID PINACOL ESTER

98%

Reagent Code: #214242
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CAS Number 940284-18-4

science Other reagents with same CAS 940284-18-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.14 g/mol
Formula C₁₁H₁₇BN₂O₂S
badge Registry Numbers
MDL Number MFCD07781247
thermostat Physical Properties
Melting Point 73-78 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl systems found in active pharmaceutical ingredients. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for developing kinase inhibitors and other heterocyclic compounds. The methylthio group can act as a directing group or be further modified to thioether, sulfoxide, or sulfone functionalities, adding versatility in late-stage functionalization. Commonly employed in the development of agrochemicals and medicinal chemistry research due to its stability and reactivity profile.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿26,130.00
2-(METHYLTHIO)PYRIMIDINE-5-BORONIC ACID PINACOL ESTER
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Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl systems found in active pharmaceutical ingredients. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for developing kinase inhibitors and other heterocyclic compounds. The methylthio group can act as a directing group or be further modified to thioether, sulfoxide, or sulfone functionalities, a

Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl systems found in active pharmaceutical ingredients. Its boronic ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for developing kinase inhibitors and other heterocyclic compounds. The methylthio group can act as a directing group or be further modified to thioether, sulfoxide, or sulfone functionalities, adding versatility in late-stage functionalization. Commonly employed in the development of agrochemicals and medicinal chemistry research due to its stability and reactivity profile.

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