
CAS 1104637-53-7
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5 produits concernés.
Ethynylboronic acid MIDA ester
CAS :Formule :C7H8BNO4Degré de pureté :90%Couleur et forme :SolidMasse moléculaire :180.9537Boron, [N-[(carboxy-κO)methyl]-N-methylglycinato(2-)-κN,κO]ethynyl-, (T-4)-
CAS :Boron, [N-[(carboxy-κO)methyl]-N-methylglycinato(2-)-κN,κO]ethynyl-, (T-4)-Degré de pureté :90% (stabilized with 200-300ppm TBC)Masse moléculaire :180.95g/molETHYNYLBORONIC ACID MIDA ESTER
CAS :Formule :C7H8BNO4Degré de pureté :90% (stabilized with 200-300ppm TBC)Masse moléculaire :180.95Ethynylboronic Acid MIDA Ester (>90%)
CAS :Produit contrôlé<p>Applications Ethynylboronic Acid MIDA Ester is a useful reagent in preparatino of borono-substited 1(2H)-isoquinolinones by rhodium-catalyzed cycloaddition.<br>References Wang, H., et al.: J. Am. Chem. Soc., 134, 19592 (2012);<br></p>Formule :C7H8BNO4Degré de pureté :>90%Couleur et forme :NeatMasse moléculaire :180.95Ethynylboronic acid mida ester
CAS :<p>Ethynylboronic acid mida ester is a molecule that contains a triazole or isoxazole as its central core. It can be used to synthesize isoxazoles, furopyridines, and benzofurans. The synthesis of this molecule has been shown to proceed through the use of a slow-release heterocycle that reacts with an alkyne to form an intermediate. This intermediate then undergoes cross-coupling reactions with terminal alkynes and boronic acid derivatives to produce the desired product. Modular substitution reactions have been shown to be possible on these molecules in order to obtain different products with similar structures.</p>Formule :C7H8BNO4Degré de pureté :Min. 95%Masse moléculaire :180.96 g/mol





