Phenyl-D5-boronic acid

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Phenyl-D5-boronic acid, a compound of significance in various scientific and industrial applications, stands out for its unique properties and versatile nature. This chemical entity, distinguished by the presence of deuterium at specific positions in its molecular structure, has garnered attention for its potential contributions to diverse fields. In this exploration, we delve into the bulk applications, the exclusive use in only lists of similar chemical names, and the distinctive characteristics that define Phenyl-D5-boronic acid.



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Chemical Properties: Phenyl-D5-boronic acid


Product Name Phenyl-D5-boronic acid
CAT No. CS-BX-00365
CAS No. 215527-70-1
Category Stable Isotopes
Stock IN-Stock
Mol. Wt. 126.96 g/mol
Mol. For. C₆H₂D₅BO₂
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys B(C1=CC=CC=C1)(O)O
Canonical Smiles B(C1=CC=CC=C1)(O)O
InchIKey HXITXNWTGFUOAU-RALIUCGRSA-N
Inchl InChI=1S/C6H7BO2/c8-7(9)6-4-2-1-3-5-6/h1-5,8-9H/i1D,2D,3D,4D,5D
IUPAC (2,3,4,5,6-pentadeuteriophenyl)boronic acid
Controlled No
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Phenyl-D5-boronic acid is a deuterated form of phenylboronic acid, which is widely used in organic synthesis as a reagent for the formation of carbon-carbon bonds. The compound has the molecular formula C6D5B(OH)2, with a molecular weight of 140.93 g/mol. The deuterated form, Phenyl-D5-boronic acid has a purity of at least 98% and is a white crystalline powder. Phenyl-D5-boronic acid is commonly used as a reagent for Suzuki coupling reactions, which involve the coupling of an arylboronic acid with an aryl halide in the presence of a palladium catalyst. This coupling reaction is widely used in pharmaceutical, agrochemical, and materials science research, where it is used to synthesize complex organic molecules. Phenyl-D5-boronic acid is also used in the synthesis of biologically active compounds, such as enzyme inhibitors, receptor antagonists, and anticancer agents. The deuterated form of phenylboronic acid is used in research to study the mechanism of enzyme-catalyzed reactions, where it acts as a probe to detect the formation of boronic acid esters. In conclusion, Phenyl-D5-boronic acid is a valuable reagent in organic synthesis, particularly in the formation of carbon-carbon bonds. Its use in the synthesis of biologically active compounds and in enzyme-catalyzed reactions makes it a versatile compound in medicinal chemistry research.

How is Phenyl-D5-boronic acid used ?


Phenyl-D5-boronic acid is primarily used in Electronics OLED Industry.



Synonyms


    • Phenylboronic Acid-D5
    • Phenyl-D5-boric acid
    • C6D5B(OH)2
    • Deuterated Phenylboronic Acid
    • Benzene-d5-boronic Acid
    • Boronic Acid, Phenyl-D5
    • Phenylboronic Acid, D5-labeled
    • D5-Phenylboronic Acid
    • Benzeneboronic Acid-d5


Related Compounds

Isopropanol D7 | Aniline D5 | Benzaldehyde D5 | Iodomethane-d3 | Acetone D6 | Dimethylamine D6 Hydrochloride | Bromocyclopentane D9 | Benzene D6 D-Atom 99.5% | Catechol D4 | Tert-butyl Alcohol-OD | Formic Acid-d2 | tert-Butyl-d9-amine | Acetylaniline D5 | Tert-butanol-d10 | Dibromomethane D2 | Trifluoroacetic acid-D | Phenol D5 | Bromobenzene D5 | Phenethylamine D4 HCl | tert-Butanol-d9 | Benzene-d6 | Benzoic Acid D5 | Diethyl Methyl-d3-malonate | Ethylene-d4 Glycol | Nitrobenzene D5 | Ammoninum D4 Deuteroxide | Methyl Alcohol D4 | Acetic Acid D4 | Chlorobenzene D5 | Sulfuric Acid D2 | Acetophenone D5 | Deuterium Chloride | Ethanol-OD | Methyl-D3 Amine Hydrochloride | Deuterium Bromide |

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