Boronic Acids
Items 301 to 307 of 307 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(1E)-Hept-1-en-1-ylboronic acid | 57404-76-9 | sc-258980 sc-258980A sc-258980B | 1 g 5 g 25 g | $126.00 $373.00 $1503.00 | ||
(1E)-Hept-1-en-1-ylboronic acid is characterized by its unique ability to form stable complexes with diols, facilitating the formation of boronate esters. This compound exhibits regioselectivity in cross-coupling reactions, driven by its unsaturated alkene, which can participate in various addition reactions. Its boronic acid functionality allows for reversible interactions with Lewis bases, influencing reaction dynamics and selectivity in synthetic pathways. | ||||||
4-Aminophenylboronic acid pinacol ester hydrochloride | 616227-14-6 | sc-481820 sc-481820A | 1 g 5 g | $90.00 $159.00 | ||
4-Aminophenylboronic acid pinacol ester hydrochloride exhibits unique reactivity due to its boronic acid functionality, which enables selective interactions with diols and sugars, forming stable boronate esters. This compound's pinacol ester structure enhances its stability and solubility in organic solvents, facilitating its use in cross-coupling reactions. Its ability to participate in dynamic covalent chemistry allows for the exploration of reversible binding mechanisms, making it a versatile tool in synthetic organic chemistry. | ||||||
Benzylboronic acid | 4463-42-7 | sc-483495 sc-483495A | 1 g 5 g | $255.00 $959.00 | ||
Benzylboronic acid is characterized by its unique ability to form reversible covalent bonds with diols, facilitating the development of dynamic covalent chemistry. Its boron atom exhibits Lewis acidity, allowing it to participate in nucleophilic addition reactions. The presence of the benzyl group enhances its solubility in organic solvents, while the acid's reactivity is influenced by steric and electronic factors, making it a versatile reagent in various synthetic pathways. | ||||||
2-Phenoxypyridine-5-boronic acid | 1270921-80-6 | sc-507377 | 1 g | $600.00 | ||
4-(2-Ethoxy-2-oxoethoxy)phenylboronic acid, pinacol ester | 269410-28-8 | sc-310897 sc-310897A | 1 g 5 g | $200.00 $772.00 | ||
4-(2-Ethoxy-2-oxoethoxy)phenylboronic acid, pinacol ester, showcases remarkable reactivity through its boronic acid functionality, which engages in reversible covalent bonding with diols and other nucleophiles. This compound's unique esterification enhances its stability while allowing for selective interactions in cross-coupling reactions. Its ability to form stable complexes with various substrates facilitates efficient pathways for carbon-carbon bond formation, making it a key player in synthetic organic chemistry. | ||||||
(3-Phenylaminocarbonyl)benzeneboronic acid | 397843-71-9 | sc-261105 sc-261105A | 500 mg 1 g | $276.00 $443.00 | ||
(3-Phenylaminocarbonyl)benzeneboronic acid exhibits intriguing reactivity due to its boronic acid moiety, which can form dynamic covalent bonds with a range of electrophiles. The presence of the phenylamino group enhances its electron-donating properties, promoting nucleophilic attack in various coupling reactions. This compound's ability to stabilize intermediates through π-π stacking interactions allows for efficient reaction kinetics, making it a versatile tool in organic synthesis. | ||||||
2-Anthraceneboronic Acid | 141981-64-8 | sc-472484 | 250 mg | $600.00 | ||
2-Anthraceneboronic Acid showcases unique reactivity attributed to its boronic acid functional group, which readily engages in reversible covalent bonding with electrophiles. The anthracene moiety contributes to significant π-π stacking interactions, enhancing molecular stability and facilitating efficient energy transfer. This compound's distinct electronic properties enable selective reactivity in cross-coupling reactions, making it a noteworthy participant in complex organic transformations. | ||||||