Butriptyline

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

2- tert -Butylaniline is a sterically hindered aniline. 2- tert -Butylaniline participates in chemo- and regioselective copper-catalyzed cross-coupling reaction for the effective amination of 2-chlorobenzoic acids.

Schiff base formation reaction between 4- tert -butylaniline and 4- tert -butylbenzaldehyde in ethanol has been carried out using the matrix-assisted laser desorption ionization-chip system . Application 4- tert -Butylaniline was used in the

Schiff base formation reaction between 4- tert -butylaniline and 4- tert -butylbenzaldehyde in ethanol has been carried out using the matrix-assisted laser desorption ionization-chip system . Application 4- tert -Butylaniline was used in the

Application D -Proline is a key starting material in the total synthesis of (&#8722)-secu&#8242amamine A and ( R )-harmicine. It can be used as a ligand for the synthesis of chiral polyoxometalate (POM) clusters.

Application D -Proline is a key starting material in the total synthesis of (&#8722)-secu&#8242amamine A and ( R )-harmicine. It can be used as a ligand for the synthesis of chiral polyoxometalate (POM) clusters.

tert -Butyl formate is an organic chemical compound obtained during the decomposition of methyl tert -butyl ether (MTBE). Application tert -Butyl formate can be used as a reagent in the direct carbonylation of benzyl halides in the presence of a

tert -Butyl formate is an organic chemical compound obtained during the decomposition of methyl tert -butyl ether (MTBE). Application tert -Butyl formate can be used as a reagent in the direct carbonylation of benzyl halides in the presence of a