2,6-Dimethylpyridin-3-ylboronic acid

95%

Reagent Code: #89596
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CAS Number 693774-55-9

science Other reagents with same CAS 693774-55-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.97 g/mol
Formula C₇H₁₀BNO₂
badge Registry Numbers
MDL Number MFCD07437925
thermostat Physical Properties
Boiling Point 295.8°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders and infections. Plays a significant role in cross-coupling reactions, such as Suzuki-Miyaura reactions, to create complex organic compounds. Applied in material science for the preparation of advanced polymers and ligands in catalysis. Also utilized in agrochemical research for designing novel pesticides and herbicides. Its boronic acid group enables efficient conjugation and modification in various chemical processes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿3,114.00
100mg
10-20 days ฿11,124.00
2,6-Dimethylpyridin-3-ylboronic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders and infections. Plays a significant role in cross-coupling reactions, such as Suzuki-Miyaura reactions, to create complex organic compounds. Applied in material science for the preparation of advanced polymers and ligands in catalysis. Also utilized in agrochemical research for designing novel pesticides and herbicides. Its boronic acid group enables efficient conjugat

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting neurological disorders and infections. Plays a significant role in cross-coupling reactions, such as Suzuki-Miyaura reactions, to create complex organic compounds. Applied in material science for the preparation of advanced polymers and ligands in catalysis. Also utilized in agrochemical research for designing novel pesticides and herbicides. Its boronic acid group enables efficient conjugation and modification in various chemical processes.

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