(2-Chloro-6-isopropylpyridin-3-yl)boronic acid

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Reagent Code: #163963
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CAS Number 1003043-37-5

science Other reagents with same CAS 1003043-37-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.445 g/mol
Formula C₈H₁₁BClNO₂
badge Registry Numbers
MDL Number MFCD08274472
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, especially in Suzuki-Miyaura cross-coupling reactions to construct carbon-carbon bonds. Its boronic acid functionality allows for efficient and selective coupling with aryl or heteroaryl halides, making it valuable in the development of crop protection agents and bioactive molecules. The presence of the chloro and isopropyl groups on the pyridine ring enhances its utility in creating structurally diverse compounds with targeted biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,020.00
inventory 1g
10-20 days ฿3,840.00
inventory 5g
10-20 days ฿17,500.00

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(2-Chloro-6-isopropylpyridin-3-yl)boronic acid
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Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, especially in Suzuki-Miyaura cross-coupling reactions to construct carbon-carbon bonds. Its boronic acid functionality allows for efficient and selective coupling with aryl or heteroaryl halides, making it valuable in the development of crop protection agents and bioactive molecules. The presence of the chloro and isopropyl groups on the pyridine ring enhances its utility in creating structurally diverse compounds

Used primarily as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, especially in Suzuki-Miyaura cross-coupling reactions to construct carbon-carbon bonds. Its boronic acid functionality allows for efficient and selective coupling with aryl or heteroaryl halides, making it valuable in the development of crop protection agents and bioactive molecules. The presence of the chloro and isopropyl groups on the pyridine ring enhances its utility in creating structurally diverse compounds with targeted biological activity.

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