1-(Triisopropylsilyl)pyrrole-3-boronic acid

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Reagent Code: #89484
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CAS Number 138900-55-7

science Other reagents with same CAS 138900-55-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.25 g/mol
Formula C₁₃H₂₆BNO₂Si
badge Registry Numbers
MDL Number MFCD01114667
thermostat Physical Properties
Boiling Point 337.9°C
inventory_2 Storage & Handling
Density 0.96g/mL
Storage  2-8°C

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the formation of carbon-carbon bonds, particularly in the synthesis of complex organic molecules. Its application is significant in the pharmaceutical industry for creating active pharmaceutical ingredients (APIs) and intermediates. It also plays a role in material science for developing advanced polymers and organic electronic materials. The triisopropylsilyl group enhances stability and selectivity during reactions, making it valuable in precision organic synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿18,720.00
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1-(Triisopropylsilyl)pyrrole-3-boronic acid
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the formation of carbon-carbon bonds, particularly in the synthesis of complex organic molecules. Its application is significant in the pharmaceutical industry for creating active pharmaceutical ingredients (APIs) and intermediates. It also plays a role in material science for developing advanced polymers and organic electronic materials. The triisopropylsilyl group enhances stability and selectivity during reactions, making

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the formation of carbon-carbon bonds, particularly in the synthesis of complex organic molecules. Its application is significant in the pharmaceutical industry for creating active pharmaceutical ingredients (APIs) and intermediates. It also plays a role in material science for developing advanced polymers and organic electronic materials. The triisopropylsilyl group enhances stability and selectivity during reactions, making it valuable in precision organic synthesis.

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