Oxiranyl boronic acid MIDA ester

95%

Reagent Code: #221968
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CAS Number 1152427-91-2

science Other reagents with same CAS 1152427-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.97 g/mol
Formula C₇H₁₀BNO₅
badge Registry Numbers
MDL Number MFCD16875672
thermostat Physical Properties
Melting Point 188-193℃
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions as a stable boron reagent, enabling efficient synthesis of complex organic molecules. Its MIDA ester group enhances stability and solubility, allowing for iterative cross-coupling strategies in natural product synthesis. The oxirane ring can undergo selective ring-opening reactions, making it valuable for building polyfunctionalized structures in pharmaceutical and agrochemical research. Ideal for modular synthesis due to its compatibility with various functional groups and reaction conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿12,620.00
5g
10-20 days ฿61,270.00
Oxiranyl boronic acid MIDA ester
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Used in Suzuki-Miyaura cross-coupling reactions as a stable boron reagent, enabling efficient synthesis of complex organic molecules. Its MIDA ester group enhances stability and solubility, allowing for iterative cross-coupling strategies in natural product synthesis. The oxirane ring can undergo selective ring-opening reactions, making it valuable for building polyfunctionalized structures in pharmaceutical and agrochemical research. Ideal for modular synthesis due to its compatibility with various func

Used in Suzuki-Miyaura cross-coupling reactions as a stable boron reagent, enabling efficient synthesis of complex organic molecules. Its MIDA ester group enhances stability and solubility, allowing for iterative cross-coupling strategies in natural product synthesis. The oxirane ring can undergo selective ring-opening reactions, making it valuable for building polyfunctionalized structures in pharmaceutical and agrochemical research. Ideal for modular synthesis due to its compatibility with various functional groups and reaction conditions.

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