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

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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.

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