932378-94-4

Basic information

• Product Name: 3,5-bis(ethoxycarbonyl)phenylboronicacid
• Synonyms: 3,5-bis(ethoxycarbonyl)phenylboronicacid;1,3-diethylisophthalate-5-boronic acid;(3,5-bis(ethoxycarbonyl)phenyl)boronic acid（WS202795）
• CAS NO: 932378-94-4
• Molecular Formula: C₁₂H₁₅BO₆
• Molecular Weight: 266.0549
• Mol File: 932378-94-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 452.1±55.0 °C(Predicted)
• Appearance: /
• Density: 1.25±0.1 g/cm3(Predicted)
• Solubility: soluble in Methanol
• PKA: 7.04±0.10(Predicted)
• CAS DataBase Reference: 3,5-bis(ethoxycarbonyl)phenylboronicacid(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-bis(ethoxycarbonyl)phenylboronicacid(932378-94-4)
• EPA Substance Registry System: 3,5-bis(ethoxycarbonyl)phenylboronicacid(932378-94-4)

Safety Data

• Hazardous Substances Data: 932378-94-4(Hazardous Substances Data)

Usage

General Description

3,5-bis(ethoxycarbonyl)phenylboronic acid is a chemical compound with the molecular formula C14H17BO6. It is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura cross-coupling reaction to form carbon-carbon bonds. 3,5-bis(ethoxycarbonyl)phenylboronicacid is a boronic acid derivative with two ethoxycarbonyl groups attached to a phenyl ring. It is a white to off-white solid that is sparingly soluble in water but more soluble in organic solvents. 3,5-bis(ethoxycarbonyl)phenylboronic acid is a versatile compound that is utilized in pharmaceutical and agrochemical research, as well as in the production of various organic compounds. It is important to handle this chemical with care and follow proper safety protocols due to its potential health hazards.

Upstream product

• 881302-73-4 benzene-1,3-dicarboxylic-5-boronic triacid 
• 64-17-5 ethanol 
• 368455-15-6 diethyl 5-iodo-1,3-benzenedicarboxylate 
• 42122-73-6 diethyl 5-aminoisophthalate 
• 99-31-0 5-aminoisophthalic acid 
• 172975-69-8 3,5-dimethylphenyl boronic acid 
• 556-96-7 5-bromo-1,3-xylene 
• 7722-64-7 potassium permanganate 

Downstream Products

• 1262962-06-0 pyridine-4-(phenyl-3',5'-dicarboxylic acid) 
• 2602573-59-9 4′,4?-(pyridine-3,5-diyl)bis([1,1′-biphenyl]-3,5-dicarboxylic acid) 
• 1874200-71-1 2’-amino-1,1’:4’,1’’-terphenyl-3,3’’,5,5’’-tetracarboxylicacid 
• 921619-91-2 1,1’:4’,1’’:4’’,1’’’-quaterphenyl-3,3’’’,5,5’’’-tetracarboxylic acid 

Relevant articles and documents

A highly stable terbium metal-organic framework for efficient detection of picric acid in water

A highly stable fluorescent terbium MOF (Tb4(paip)6·1.2H2O, paip = 5-(1H-pyrazole-4-yl)isophthalate) showing a sharp green emission (545 nm) and a quantum yield of 21.0% was successfully synthesized. This compound is shown

The Origin of Catalytic Benzylic C?H Oxidation over a Redox-Active Metal–Organic Framework

Selective oxidation of benzylic C?H compounds to ketones is important for the production of a wide range of fine chemicals, and is often achieved using toxic or precious metal catalysts. Herein, we report the efficient oxidation of benzylic C?H groups in a broad range of substrates under mild conditions over a robust metal–organic framework material, MFM-170, incorporating redox-active [Cu2II(O2CR)4] paddlewheel nodes. A comprehensive investigation employing electron paramagnetic resonance (EPR) spectroscopy and synchrotron X-ray diffraction has identified the critical role of the paddlewheel moiety in activating the oxidant tBuOOH (tert-butyl hydroperoxide) via partial reduction to [CuIICuI(O2CR)4] species.

Liquid phase epitaxial growth of heterostructured hierarchical MOF thin films

Precise control of epitaxial growth of MOF-on-MOF thin films, for ordered hierarchical tbo-type structures is demonstrated. The heterostructured MOF thin film was fabricated by successful sequential deposition of layers from two different MOFs. The 2-periodic layers, edge-transitive 4,4-square lattices regarded as supermolecular building layers, were commendably cross-linked using a combination of inorganic/organic and organic pillars.