Molecular structure of (1E)-(Pent-1-en-1-yl)boronic acid, CAS Number: 59239-44-0
(1E)-(Pent-1-en-1-yl)boronic acid (CAS 59239-44-0)
Alternate Names:
trans-(Pent-1-en-1-yl)boronic acid
CAS Number:
59239-44-0
Purity:
≥98%
Molecular Weight:
113.95
Molecular Formula:
C5H11BO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
(1E)-(Pent-1-en-1-yl)boronic acid is a boronic acid that can be used in palladium-, copper-, or suzuki-catalyzed coupling reactions. It is a sterically hindered and a bimetallic reagent that is useful in the synthesis of substituted boronates. (1E)-(Pent-1-en-1-yl)boronic acid functions as a Lewis acid, forming boronate esters with diverse substrates. These esters can then serve as intermediates in various chemical reactions, such as the synthesis of polymers, organometallic compounds, and other organic substances.
(1E)-(Pent-1-en-1-yl)boronic acid (CAS 59239-44-0) References
- Biomimetic electrochemical sensor for the highly selective detection of azithromycin in biological samples. | Stoian, IA., et al. 2020. Biosens Bioelectron. 155: 112098. PMID: 32090870
Inhibitor of:
Cephalosporin.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(1E)-(Pent-1-en-1-yl)boronic acid, 1 g | sc-258979 | 1 g | $69.00 | |||
(1E)-(Pent-1-en-1-yl)boronic acid, 5 g | sc-258979A | 5 g | $235.00 |