1-[(2,4-dichlorophenyl)methyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

95%

Reagent Code: #195863
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CAS Number 2246901-18-6

science Other reagents with same CAS 2246901-18-6

blur_circular Chemical Specifications

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Weight 353.05126 g/mol
Formula C₁₆H₁₉BCl₂N₂O₂
badge Registry Numbers
MDL Number MFCD21337493
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group readily reacts with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex organic molecules. It is particularly useful in medicinal chemistry for modifying pyrazole-based scaffolds, which are common in bioactive compounds. The presence of the dichlorobenzyl moiety can enhance lipophilicity and influence target binding in drug design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿22,080.00
inventory 1g
10-20 days ฿48,000.00

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1-[(2,4-dichlorophenyl)methyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group readily reacts with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex organic molecules. It is particularly useful in medicinal chemistry for modifying pyrazole-based scaffolds, which are common in bioactive compounds. The presence of the dichlorobenz

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group readily reacts with aryl or heteroaryl halides under palladium catalysis, making it valuable for constructing complex organic molecules. It is particularly useful in medicinal chemistry for modifying pyrazole-based scaffolds, which are common in bioactive compounds. The presence of the dichlorobenzyl moiety can enhance lipophilicity and influence target binding in drug design.

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