31754-00-4

Usage

Uses

Used in Chemical Testing:
3-(3-Carboxypropionylamino)phenylboronic Acid is used as a reagent in chemical testing for its unique properties and interactions with other compounds.
Used in Scientific Research:
3-(3-CARBOXYPROPIONYLAMINO)PHENYLBORONIC ACID serves as a valuable tool in scientific research, where it is employed to study various chemical reactions and processes.
Used in Pharmaceutical Development:
3-(3-Carboxypropionylamino)phenylboronic Acid is used as a potential building block in the development of pharmaceuticals, given its unique chemical structure and properties that may contribute to the creation of new drug molecules.

Upstream product

• 108-30-5 succinic acid anhydride 
• 30418-59-8 3-Aminophenylboronic acid 

Downstream Products

• 170368-32-8 N-(3-dihydroxyborylphenyl)succinamic acid hydrazide 

Relevant academic research and scientific papers

Stimuli responsive chiral liquid crystal phases of phenylboronic acid functionalized rodlike viruses and their interaction with biologically important diols

The rodlike M13 viruses with chemically decorated phenylboronic acid moieties form pH responsive chiral nematic liquid crystal (LC) phases. Binding with biologically important diols results in LC phases with microstructures that closely correlate with the molecular structure of the diols and can be conveniently discerned by visual cues. This journal is the Partner Organisations 2014.

Gels and multilayer surface structures from boronic acid containing polymers

Boronic acid containing polymers are used to form bioinert gels and multilayer surface structures. These polymers form crosslinked hydrogels, which are highly swollen in water. The crosslinking can either be chemical or physical. Water soluble polymers containing boronic acid groups, such as phenylboronic acid (PBA), can be physically crosslinked by mixing the polymers in water with other polymers containing hydroxyls or carboxylic acids. Alternatively, surfaces can be treated by stepwise incubation with a solution of the boronic acid containing polymer, followed by incubation with a solution of a diol or carboxylic acid containing polymer. Many successive layers can be generated, increasing the thickness of the formed structure at each step. The bioinert gel or surface coating can be used for passivating the surfaces of medical implants (especially those based on transplanted tissue), or for passivating the surfaces of tissues in situ, decreasing the incidence or severity of such pathologic conditions as the formation of post-surgical adhesions, and thrombosis following angioplasty.

Phenylboronic acid complexes for bioconjugate preparation

The present invention relates to a novel class of phenylboronic acid bioconjugate complexes derived from aminosalicylic acid, and the method of making and using such bioconjugate complexes. The bioconjugate complexes are in the form of the following gener