Diisopropyl (Bromomethyl)boronate

≥95%

Reagent Code: #89418
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CAS Number 137297-49-5

science Other reagents with same CAS 137297-49-5

blur_circular Chemical Specifications

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Weight 222.92 g/mol
Formula C₇H₁₆BBrO₂
badge Registry Numbers
MDL Number MFCD01631222
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a versatile reagent for introducing boron-containing functional groups into molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic compounds, such as pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the preparation of boronic esters, which are widely employed in materials science and catalysis. Its reactivity with nucleophiles makes it useful for constructing boron-based building blocks in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,214.00
inventory 1g
10-20 days ฿5,580.00

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Diisopropyl (Bromomethyl)boronate
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Used in organic synthesis as a versatile reagent for introducing boron-containing functional groups into molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic compounds, such as pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the preparation of boronic esters, which are widely employed in materials science and catalysis. Its reactivity with nucleophiles makes

Used in organic synthesis as a versatile reagent for introducing boron-containing functional groups into molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic compounds, such as pharmaceuticals and agrochemicals. Additionally, it serves as a key intermediate in the preparation of boronic esters, which are widely employed in materials science and catalysis. Its reactivity with nucleophiles makes it useful for constructing boron-based building blocks in medicinal chemistry and drug discovery.

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