Biotinyl-phenylboronic acid

Based on 8 reference(s) in Google Scholar 9 10 8

Axon 2256

CAS [1661014-48-7]

MF C16H22BN3O4S
MW 363.24

Purity: 99%
Soluble in 0.1N NaOH(aq), MeOH and DMSO

Biotinyl-phenylboronic acid

Description

Biotin functionalized arylboronic acid for the use of palladium-catalyzed oxidative Heck reaction to protein-bound alkenes and Suzuki-Miyaura cross-coupling for labeling of protein bound phenylhalides in high yields and with excellent chemoselectivity. Reagent for bio-orthogonal protein-ligation. Signal enhancement with streptavidin-HRP.

*Sold in collaboration with RuG (University of Groningen)

ME Ourailidou et al. Aqueous oxidative Heck reaction as a protein-labeling strategy. Chembiochem. 2014, 15, 209-212.

F D'Hooge et al. Biotinylated boronic acid fluorophore conjugates: Quencher elimination strategy for imaging and saccharide detection. RSC Adv. 2012, 2, 3274-3280.

Chalker et al. A Convenient Catalyst for Aqueous and Protein Suzuki-Miyaura Cross-Coupling J. Am. Chem. Soc. 2009, 131, 16346-16347

C.D. Spicer et al. Palladium-mediated site-selective Suzuki-Miyaura protein modification at genetically encoded aryl halides. Chem. Commun. 2011, 47, 1698-700

C.D. Spicer et al. Palladium-mediated cell-surface labeling. J. Am. Chem. Soc. 2012, 134(2), 800-3.

Miscellaneous Proteins RuG Collaboration Products

Biotinylated arylboronic acid for bio-orthogonal chemistry

Chemical name

3-(5-((4S)-2-Oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)phenylboronic acid

Source information

Sold in collaboration with RuG (University of Groningen)

Parent CAS No.

[1661014-48-7]

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Size	Unit Price	Stock
5 mg	€95.00	In Stock
25 mg	€285.00	In Stock

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Biotinyl-phenylboronic acid

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Biotinyl-phenylboronic acid

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Chemical name

Source information

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