Desipramine trifluoroacetate

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Application Used in the development of a microwave-mediated method for O -allylation of amido alcohols on chromatographic alumina.

N -(2-Pyridyl)bis(trifluoromethanesulfonimide) (2-[ N,N -Bis(trifluoromethylsulfonyl)amino]pyridine, N , N -Bis(trifluoromethylsulfonyl)-2-pyridylamine)) is a useful triflating reagent. It has been synthesized by reacting 2-aminopyridine and

Application As reported by the Alexanian laboratory, this reagent is used for site-selective, intermolecular decarboxylative xanthylation leading to the rapid diversification of carboxylic acids. Once installed, the xanthate group provides direct

Application Catalyst for enantioselective Michael addition . It can act as a catalyst for the asymmetric tandem aza-Michael addition-protonation between 1-nitro cyclohexene and 4-methoxyaniline to form the corresponding

Application Catalyst for enantioselective Michael addition . It can act as a catalyst for the asymmetric tandem aza-Michael addition-protonation between 1-nitro cyclohexene and 4-methoxyaniline to form the corresponding

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

N -Methyl-bis(trifluoroacetamide) is a common reagent used in the alkylation process, which targets highly polar, multi-functional compounds such as carbohydrates and amino acids. Application N -Methyl-bis(trifluoroacetamide) may be used as an

N -Methyl-bis(trifluoroacetamide) is a common reagent used in the alkylation process, which targets highly polar, multi-functional compounds such as carbohydrates and amino acids. Application N -Methyl-bis(trifluoroacetamide) may be used as an

Application Acts as a transparent strong electron-withdrawing p-type dopant in carbon nanotubes Reactant for: Synthesis of amphoteric alpha-boryl aldehydes Enantioselective synthesis of core ring skeleton of leucosceptroids A-D Stereoselective

Application Acts as a transparent strong electron-withdrawing p-type dopant in carbon nanotubes Reactant for: Synthesis of amphoteric alpha-boryl aldehydes Enantioselective synthesis of core ring skeleton of leucosceptroids A-D Stereoselective

Application Acts as a transparent strong electron-withdrawing p-type dopant in carbon nanotubes Reactant for: Synthesis of amphoteric alpha-boryl aldehydes Enantioselective synthesis of core ring skeleton of leucosceptroids A-D Stereoselective