2-(Methylethylamino-d8)-pyrimidine-5-boronic acid

95%

Reagent Code: #91544
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CAS Number 2225172-68-7

science Other reagents with same CAS 2225172-68-7

blur_circular Chemical Specifications

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Weight 189.049374224 g/mol
Formula C₇H₄BD₈N₃O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a crucial intermediate in the development of deuterated drugs, where the presence of deuterium can enhance the metabolic stability and efficacy of pharmaceutical compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in constructing complex organic molecules. Additionally, it is employed in the synthesis of pyrimidine derivatives, which are important in the creation of various bioactive molecules, including antiviral and anticancer agents.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿269,620.00
inventory 25mg
10-20 days ฿720,000.00

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2-(Methylethylamino-d8)-pyrimidine-5-boronic acid
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This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a crucial intermediate in the development of deuterated drugs, where the presence of deuterium can enhance the metabolic stability and efficacy of pharmaceutical compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in constructing complex organic molecules. Additionally, it is emp

This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a crucial intermediate in the development of deuterated drugs, where the presence of deuterium can enhance the metabolic stability and efficacy of pharmaceutical compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, which is essential in constructing complex organic molecules. Additionally, it is employed in the synthesis of pyrimidine derivatives, which are important in the creation of various bioactive molecules, including antiviral and anticancer agents.

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