Discovery of Benzo[b]furan-2-carboxaldehyde

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 4265-16-1, you can also check out more blogs about4265-16-1

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Product Details of 4265-16-1. Introducing a new discovery about 4265-16-1, Name is Benzo[b]furan-2-carboxaldehyde

A simple, mild, and practical process for direct conversion of aldehydes to nitriles was developed feathering a wide substrate scope and great functional group tolerability (52 examples, over 90% yield in most cases) using inorganic reagents (NH2OH/Na2CO3/SO2F2) in DMSO. This method allows for transformations of readily available, inexpensive, and abundant aldehydes to highly valuable nitriles in a pot, atom, and step-economical manner without transition metals. This protocol will serve as a robust tool for the installation of cyano-moieties to complicated molecules.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 4265-16-1, you can also check out more blogs about4265-16-1

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H815O – PubChem