(4-(((2,5-Dioxopyrrolidin-1-yl)oxy)carbonyl)phenyl)boronic acid

95%

Reagent Code: #89169
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CAS Number 159276-65-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.01 g/mol
Formula C₁₁H₁₀BNO₆
badge Registry Numbers
MDL Number MFCD28955537
thermostat Physical Properties
Boiling Point 483.0±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.51±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily used in the field of organic synthesis and bioconjugation. It serves as a versatile reagent for the modification of biomolecules, particularly in the preparation of boron-containing compounds. The boronic acid group enables its application in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, it is utilized in the development of targeted drug delivery systems, where it can be conjugated to drugs or imaging agents to enhance specificity towards certain biological targets. Its reactive N-hydroxysuccinimide (NHS) ester moiety allows for efficient coupling with amines, making it valuable for labeling proteins, peptides, and other amine-containing molecules in biochemical research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $183.36
inventory 250mg
10-20 days $333.39
inventory 1g
10-20 days $666.77
(4-(((2,5-Dioxopyrrolidin-1-yl)oxy)carbonyl)phenyl)boronic acid
This chemical is primarily used in the field of organic synthesis and bioconjugation. It serves as a versatile reagent for the modification of biomolecules, particularly in the preparation of boron-containing compounds. The boronic acid group enables its application in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, it is utilized in the development of targeted drug delivery systems, where it can be conjugated to drugs or imaging agents to enhance specificity towards certain biological targets. Its reactive N-hydroxysuccinimide (NHS) ester moiety allows for efficient coupling with amines, making it valuable for labeling proteins, peptides, and other amine-containing molecules in biochemical research.
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