4-Chloro-2-(cyclopropyl)pyrimidine-5-boronic acid

95%

Reagent Code: #60897
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CAS Number 2225177-67-1

science Other reagents with same CAS 2225177-67-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.41462 g/mol
Formula C₇H₈BClN₂O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis as a versatile building block for the preparation of complex molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the development of drugs targeting various diseases, including cancer and infectious diseases. The boronic acid group enables efficient cross-coupling reactions, such as Suzuki-Miyaura reactions, to form carbon-carbon bonds, which are crucial in constructing biologically active compounds. Its pyrimidine core is a common motif in medicinal chemistry, often incorporated into molecules with therapeutic potential. Additionally, the cyclopropyl group can enhance the metabolic stability and binding affinity of the final drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿29,304.00
5mg
10-20 days ฿10,080.00

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4-Chloro-2-(cyclopropyl)pyrimidine-5-boronic acid
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Used in organic synthesis as a versatile building block for the preparation of complex molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the development of drugs targeting various diseases, including cancer and infectious diseases. The boronic acid group enables efficient cross-coupling reactions, such as Suzuki-Miyaura reactions, to form carbon-carbon bonds, which are crucial in constructing biologically active compounds. Its pyrimidine core is a common motif in med
Used in organic synthesis as a versatile building block for the preparation of complex molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the development of drugs targeting various diseases, including cancer and infectious diseases. The boronic acid group enables efficient cross-coupling reactions, such as Suzuki-Miyaura reactions, to form carbon-carbon bonds, which are crucial in constructing biologically active compounds. Its pyrimidine core is a common motif in medicinal chemistry, often incorporated into molecules with therapeutic potential. Additionally, the cyclopropyl group can enhance the metabolic stability and binding affinity of the final drug candidates.
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