3-Chloro-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

98%

Reagent Code: #164932
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CAS Number 2271133-59-4

science Other reagents with same CAS 2271133-59-4

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research. The presence of the chloro and amide functionalities allows for further selective modifications, supporting its use in the development of bioactive compounds and functional materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,950.00
1g
10-20 days ฿7,260.00
5g
10-20 days ฿25,400.00
100mg
10-20 days ฿780.00

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3-Chloro-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research. The presence of the chloro and amide functionalities allows for further selective modifications, supporting its use in the development of bioactive compounds and
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research. The presence of the chloro and amide functionalities allows for further selective modifications, supporting its use in the development of bioactive compounds and functional materials.
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