4-Methyl-2-(1H-pyrazol-1-yl)pyrimidine-5-boronic acid

95%

Reagent Code: #92189
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CAS Number 2225179-93-9

science Other reagents with same CAS 2225179-93-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.99366 g/mol
Formula C₈H₉BN₄O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various heterocyclic compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules for drug development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the construction of carbon-carbon bonds. This compound is also utilized in the synthesis of biologically active molecules, including potential therapeutic agents targeting specific enzymes or receptors. Additionally, it finds applications in material science for the development of organic electronic materials and polymers.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿29,700.00
inventory 100mg
10-20 days ฿82,800.00

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4-Methyl-2-(1H-pyrazol-1-yl)pyrimidine-5-boronic acid
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Used in organic synthesis as a key intermediate for the preparation of various heterocyclic compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules for drug development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the construction of carbon-carbon bonds. This compound is also utilized in the synthesis of biologically active molecules, including potential th

Used in organic synthesis as a key intermediate for the preparation of various heterocyclic compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules for drug development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the construction of carbon-carbon bonds. This compound is also utilized in the synthesis of biologically active molecules, including potential therapeutic agents targeting specific enzymes or receptors. Additionally, it finds applications in material science for the development of organic electronic materials and polymers.

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