28362-31-4

Basic information

• Product Name: 1,4-Bis(dihydroxyboryl)-2-nitrobenzene
• Synonyms: (2-Nitro-1,4-phenylene)bis(dihydroxyborane);1,4-Bis(dihydroxyboryl)-2-nitrobenzene
• CAS NO: 28362-31-4
• Molecular Formula: C₆H₇B₂NO₆
• Molecular Weight: 210.7449
• Mol File: 28362-31-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 507.5°Cat760mmHg
• Flash Point: 260.7°C
• Appearance: /
• Density: 1.55g/cm³
• Vapor Pressure: 4.04E-11mmHg at 25°C
• Refractive Index: 1.589
• CAS DataBase Reference: 1,4-Bis(dihydroxyboryl)-2-nitrobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Bis(dihydroxyboryl)-2-nitrobenzene(28362-31-4)
• EPA Substance Registry System: 1,4-Bis(dihydroxyboryl)-2-nitrobenzene(28362-31-4)

Safety Data

• Hazardous Substances Data: 28362-31-4(Hazardous Substances Data)

Usage

Type of compound

Boron-containing aromatic compound

Applications

a. Synthesis of high-energy density materials
b. Precursor for organic light-emitting diodes (OLEDs)
c. Materials science and organic electronics
d. Fluorescent sensors and imaging agents for biological and medical applications
e. Reagent in organic synthesis
f. Building block for boron-containing compounds with specific properties and functions

Structure

Unique arrangement of atoms that contributes to its properties and potential applications

Properties

a. Stability in various environments
b. Reactivity with other compounds for synthesis purposes
c. Fluorescent properties for sensing and imaging applications
d. High-energy density for use in energy storage materials

Potential

Promising candidate for various applications due to its structure and properties

InChI:InChI=1/C6H7B2NO6/c10-7(11)4-1-2-5(8(12)13)6(3-4)9(14)15/h1-3,10-13H

Upstream product

• 106-37-6 1.4-dibromobenzene 
• 4612-26-4 1,4-Phenyldiboronic acid 

Relevant articles and documents

Side functionalization of diboronic acid precursors for covalent organic frameworks

A series of substituted 1,4-benzenediboronic acids (BDBA) was synthesized and their thermal properties investigated. Two diboronic acids were studied as building-blocks for covalent organic framework (COF) formation, namely 2,5-dimethoxy-1,4-benzenediboronic acid and 2-nitro-1,4-benzeneboronic acid. Interestingly, substitution of the BDBA core caused a dramatic decrease of the polymerization temperature leading to the formation of a less organized structure.