Molecular structure of 2-Benzofuranylboronic acid, CAS Number: 98437-24-2
2-Benzofuranylboronic acid (CAS 98437-24-2)
Alternate Names:
2-Benzofuranboronic acid; Benzofuran-2-ylboronic acid
CAS Number:
98437-24-2
Molecular Weight:
161.95
Molecular Formula:
C8H7BO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
Contains varying amounts of anhydride. 2-Benzofuranylboronic acid is an organic compound derived from benzofuran and boronic acid, belonging to the family of heterocyclic compounds. Its versatility is observed as a building block in the synthesis of diverse natural products. Furthermore, it plays a role in the development of innovative materials, including polymers and nanomaterials. Additionally, it finds applications in the synthesis of fluorescent dyes and other compounds used for imaging and spectroscopy purposes.
2-Benzofuranylboronic acid (CAS 98437-24-2) References
- The palladium-catalyzed addition of organoboronic acids to alkynes. | Oh, CH., et al. 2003. Angew Chem Int Ed Engl. 42: 805-8. PMID: 12596206
- A new structural theme in C2-symmetric HIV-1 protease inhibitors: ortho-substituted P1/P1' side chains. | Wannberg, J., et al. 2006. Bioorg Med Chem. 14: 5303-15. PMID: 16621572
- Semisynthetic neoclerodanes as kappa opioid receptor probes. | Lovell, KM., et al. 2012. Bioorg Med Chem. 20: 3100-10. PMID: 22464684
- Toward highly potent cancer agents by modulating the C-2 group of the arylthioindole class of tubulin polymerization inhibitors. | La Regina, G., et al. 2013. J Med Chem. 56: 123-49. PMID: 23214452
- Transitioning organic synthesis from organic solvents to water. What's your E Factor? | Lipshutz, BH. and Ghorai, S. 2014. Green Chem. 16: 3660-3679. PMID: 25170307
- Palladium-Catalyzed Arylation of Arylboronic Acids with Yagupolskii-Umemoto Reagents. | Wang, SM., et al. 2016. Chemistry. 22: 6542-6. PMID: 26946261
- Alkyne Benzannulation Reactions for the Synthesis of Novel Aromatic Architectures. | Hein, SJ., et al. 2017. Acc Chem Res. 50: 2776-2788. PMID: 29112367
- Nickel-Catalyzed Radical Migratory Coupling Enables C-2 Arylation of Carbohydrates. | Zhao, G., et al. 2021. J Am Chem Soc. 143: 8590-8596. PMID: 34086440
- Synthesis and biological evaluation of selected 7H-pyrrolo[2,3-d]pyrimidine derivatives as novel CDK9/CyclinT and Haspin inhibitors. | Pieterse, L., et al. 2021. Chem Biol Interact. 349: 109643. PMID: 34508710
- Synthesis and reactivity of 5-Br(I)-indolizines and their parallel cross-coupling reactions | Alexey G. Kuznetsov, Alexander A. Bush, Eugene V. Babaev. 2008. Tetrahedron. 64: 749-756.
- Diastereoselective addition to N-acyliminium ions with aryl- and alkenyl boronic acids via a Petasis-type reaction | Satoshi Mizuta and Osamu Onomura *. 2012. RSC Adv. 2: 2266-2269.
- Synthesis of fluorinated oxygen- and sulfur-containing heteroaromatics | Eileen M. O'Leary a b c, David J. Jones a c, Fíona P. O'Donovan a c, Timothy P. O'Sullivan a b c. 2015. Journal of Fluorine Chemistry. 176: 93-120.
- Metal-free allylation of electron-rich heteroaryl boronic acids with allylic alcohols | Xue-Dong Li a b, Li-Jun Xie a b, De-Long Kong a b, Li Liu a, Liang Cheng a. 2016. Tetrahedron. 72: 1873-1880.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Benzofuranylboronic acid, 5 g | sc-251699 | 5 g | $120.00 |