(4-(((2,5-Dioxopyrrolidin-1-yl)oxy)carbonyl)phenyl)boronic acid
95%
Reagent
Code: #89169
CAS Number
159276-65-0
blur_circular Chemical Specifications
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Molecular Information
Weight
263.01 g/mol
Formula
C₁₁H₁₀BNO₆
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Registry Numbers
MDL Number
MFCD28955537
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Physical Properties
Boiling Point
483.0±55.0 °C(Predicted)
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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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(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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