116378-40-6

Basic information

• Product Name: 3-Amino-5-carboxylphenylboronic acid
• Synonyms: 3-AMINO-5-CARBOXYLPHENYLBORONIC ACID;(3-AMINO-5-CARBOXYPHENYL)BORONIC ACID;3-AMINO-5-BORONOBENZOIC ACID;3-Amino-5-carboxybenzeneboronic acid;3-Amino-5-carboxybenzeneboronic acid 98%;Benzoic acid, 3-aMino-5-borono;3-Amino-5-carboxybenzeneboronicacid98%
• CAS NO: 116378-40-6
• Molecular Formula: C₇H₈BNO₄
• Molecular Weight: 180.95
• Product Categories: Amines;blocks;BoronicAcids;Carboxes;Boronic acids
• Mol File: 116378-40-6.mol

Chemical Properties

• Melting Point: 210-212
• Boiling Point: 545.498 °C at 760 mmHg
• Flash Point: 283.707 °C
• Appearance: /
• Density: 1.491 g/cm³
• Vapor Pressure: 9.86E-13mmHg at 25°C
• Refractive Index: 1.63
• Storage Temp.: 2-8°C
• PKA: 3.35±0.10(Predicted)
• CAS DataBase Reference: 3-Amino-5-carboxylphenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Amino-5-carboxylphenylboronic acid(116378-40-6)
• EPA Substance Registry System: 3-Amino-5-carboxylphenylboronic acid(116378-40-6)

Safety Data

• Hazardous Substances Data: 116378-40-6(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
3-Amino-5-carboxylphenylboronic acid serves as a key building block in organic synthesis, enabling the creation of various biologically active molecules and pharmaceutical intermediates. Its presence of both amino and carboxylic acid groups allows for versatile chemical reactions and modifications, contributing to the synthesis of complex organic compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-Amino-5-carboxylphenylboronic acid is utilized for the development of new drugs and therapeutic agents. Its ability to bind to specific molecular targets makes it a promising candidate for the treatment of certain diseases, such as cancer and diabetes. Researchers leverage its chemical properties to design and optimize drug candidates with improved efficacy and selectivity.
Used in Sensor Development:
3-Amino-5-carboxylphenylboronic acid is employed in the development of sensors and chemosensors for detecting and measuring specific molecules in biological and environmental samples. Its boronic acid group can form reversible covalent bonds with diols, making it an ideal component for the design of sensors that selectively recognize and respond to specific analytes.
Used in the Treatment of Diseases:
3-Amino-5-carboxylphenylboronic acid has been studied for its potential applications in the treatment of certain diseases, such as cancer and diabetes. Its ability to bind to specific molecular targets involved in these conditions makes it a promising therapeutic agent. Researchers are exploring its potential to modulate biological pathways and develop targeted treatments for various diseases.
Used in Materials Science:
In the field of materials science, 3-Amino-5-carboxylphenylboronic acid is utilized for the development of novel materials with specific properties. Its chemical structure allows for the creation of materials with tailored characteristics, such as improved sensitivity, selectivity, or stability, which can be applied in various applications, including environmental monitoring, diagnostics, and therapeutics.

InChI:InChI=1/C7H8BNO4/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3,12-13H,9H2,(H,10,11)

Upstream product

• 25487-66-5 3-Carboxyphenylboronic acid 
• 101084-81-5 (3-carboxy-5-nitrophenyl)boronic acid 

Downstream Products

• 1009094-21-6 C₅₃H₈₂N₆O₉SSi 
• 1009094-34-1 C₅₂H₇₈N₈O₆Si 
• 1009094-19-2 C₅₂H₇₉N₅O₇Si 
• 1009094-20-5 C₄₇H₆₈N₆O₉S 
• 1009094-35-2 C₄₆H₆₄N₈O₆ 
• 1009094-40-9 C₄₆H₆₄N₆O₇ 
• 1009094-39-6 C₄₇H₆₆N₆O₇ 
• 1009094-38-5 C₄₈H₆₈N₆O₇ 
• 1009094-36-3 C₄₆H₆₃N₅O₈ 
• 1009094-32-9 C₄₆H₆₆N₆O₆ 
• 1009094-15-8 C₄₆H₆₅N₅O₇ 
• 1009094-33-0 C₄₁H₆₂N₆O₇Si 
• 1009094-37-4 C₄₄H₆₁N₅O₆ 
• 1009094-18-1 C₄₁H₆₃N₃O₈Si 

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