(1,2-dihydro-2-oxo-5-Pyrimidinyl)-boronic acid

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Reagent Code: #91810
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CAS Number 373384-19-1

science Other reagents with same CAS 373384-19-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.9051 g/mol
Formula C₄H₅BN₂O₃
badge Registry Numbers
MDL Number MFCD08275734
thermostat Physical Properties
Boiling Point 530℃at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

(1,2-dihydro-2-oxo-5-Pyrimidinyl)-boronic acid is primarily used in organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of various biologically active compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in drug discovery and material science. This compound is also utilized in the preparation of pyrimidine derivatives, which are essential in creating antiviral, anticancer, and anti-inflammatory agents. Additionally, its role in the synthesis of nucleoside analogs highlights its importance in medicinal chemistry for designing therapeutic agents targeting genetic disorders and viral infections.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿4,590.00
inventory 25mg
10-20 days ฿13,788.00
inventory 100mg
10-20 days ฿41,400.00

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(1,2-dihydro-2-oxo-5-Pyrimidinyl)-boronic acid
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(1,2-dihydro-2-oxo-5-Pyrimidinyl)-boronic acid is primarily used in organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of various biologically active compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in drug discovery and material science. This compound is also utilized in the preparation of pyrimidine derivatives, which are essential in

(1,2-dihydro-2-oxo-5-Pyrimidinyl)-boronic acid is primarily used in organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of various biologically active compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in drug discovery and material science. This compound is also utilized in the preparation of pyrimidine derivatives, which are essential in creating antiviral, anticancer, and anti-inflammatory agents. Additionally, its role in the synthesis of nucleoside analogs highlights its importance in medicinal chemistry for designing therapeutic agents targeting genetic disorders and viral infections.

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