Phenyl-D5-boronic acid, also known as deuterated phenylboronic acid (C6D5B(OH)2), is a compound in which some of the hydrogen atoms in phenylboronic acid are replaced with deuterium (a stable isotope of hydrogen). This modification can be useful in various applications in chemistry and related fields. Here are some common applications for Phenyl-D5-boronic acid:
1. Organic Synthesis: Deuterated boronic acids like Phenyl-D5-boronic acid can be used in organic synthesis as boron-containing reagents. They are particularly valuable in Suzuki-Miyaura cross-coupling reactions, allowing for the incorporation of deuterium into organic molecules.
2. Isotope Labeling: Phenyl-D5-boronic acid can serve as an isotopic label in chemical and biochemical studies. It can be used to trace the behavior and pathways of molecules in reactions, metabolic pathways, or biological systems.
3. NMR Spectroscopy: Deuterated boronic acids are often used as NMR solvents or reference compounds. They provide sharp NMR signals and can serve as standards for chemical shifts, facilitating the analysis and characterization of other compounds, especially those involving boron chemistry.
4. Spectroscopic Analysis: Phenyl-D5-boronic acid can be employed in various spectroscopic techniques, including infrared (IR) and Raman spectroscopy, where it can serve as a reference material or standard for calibration. Its distinct spectral properties can assist in characterizing other compounds.
5. Chemical Research: Researchers may use Phenyl-D5-boronic acid as a reactant or reagent in chemical reactions, particularly those involving boron-containing compounds. Its deuterium substitution can affect reaction pathways and mechanisms, making it valuable in mechanistic studies.
6. Pharmaceutical Research: It may find applications in pharmaceutical research, particularly in the development and analysis of drug compounds. Isotopic labeling can help in tracking specific functional groups in drug molecules.
7. Catalysis: Deuterated boronic acids can serve as catalysts or ligands in various catalytic reactions, influencing the selectivity and efficiency of these processes.
8. Analytical Chemistry: In some cases, Phenyl-D5-boronic acid or its derivatives can be used as internal standards or reference compounds in analytical chemistry, ensuring accurate quantification of boron-containing compounds in samples.
The choice to use Phenyl-D5-boronic acid or any deuterated compound depends on the specific requirements of the experiment or analysis and should be made with consideration of safety and regulatory guidelines.
Pub Chem
https://pubchem.ncbi.nlm.nih.gov/substance/387216364
(~2~H_5_)Phenylboronic acid
https://comptox.epa.gov/dashboard/DTXSID20584110
CompTox Chemicals Dashboard Chemical Lists
https://comptox.epa.gov/dashboard/chemical-lists/
Phenyl-d5-boronic acid
https://echa.europa.eu/information-on-chemicals
Phenyl-d5-boronic acid
https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/157083
Phenyl-d5-boronic acid
https://spectrabase.com/spectrum/4K7JG5O4QCd
GHS Classification Tree
http://www.unece.org/trans/danger/publi/ghs/ghs_welcome_e.html
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