92885-79-5

Usage

General Description

2-AMINO-N-MESITYLACETAMIDE HYDROCHLORIDE is a chemical compound that consists of an amino group, a mesityl group, and an acetamide group. It is commonly used as a reagent in organic synthesis and pharmaceutical research. The hydrochloride salt form of 2-AMINO-N-MESITYLACETAMIDE HYDROCHLORIDE is often preferred for its stability and solubility in water. It is a white or off-white crystalline powder with a melting point of approximately 150-152°C and is generally considered to be relatively stable under normal conditions. Its uses include serving as a precursor for the synthesis of various pharmaceuticals, as well as a reagent in the preparation of heterocycles and other organic compounds.

InChI:InChI=1/C11H16N2O/c1-7-4-8(2)11(9(3)5-7)13-10(14)6-12/h4-5H,6,12H2,1-3H3,(H,13,14)/p+1

Upstream product

• 88-05-1 2,4,6-trimethylaniline 

Downstream Products

• 444325-38-6 N-2,4,6-trimethylphenyl-(1,2-diaminoethane) 

Relevant academic research and scientific papers

Non covalent immobilization of pyrene-tagged ruthenium complexes onto graphene surfaces for recycling in olefin metathesis reactions

Synthesis of Hoveyda-type ruthenium complexes, modified by pyrene tags on the NHC ligand and/or the benzylidene moiety, is described. Thanks to non-covalent π-π interactions these new complexes were immobilized on carbon supports [reduced graphene oxide (rGO) or graphene] and their activity and recoverability for metatheses reactions have been studied. A SIPr-based complex possessing the pyrene function on the benzylidene ligand (C2) delivered the best results for the ring closing metathesis of diethyldiallyl malonate as benchmark reaction. The presence of additional pyrene-functionalized styrenyl-ether as ligand to the rGO-supported catalyst (C2/L@rGO) noticeably improved the recycling procedure allowing supplementary efficient catalytic runs. This may be due either to a facilitated boomerang effect or to a gradual release of the active species in solution. Finally, catalyst C2/L@rGO was proven to be successfully used to promote metathesis reactions in a multisubstrate procedure, the same supported-catalyst batch being successively engaged to transform three different substrates, in diene and ene-yne RCM reactions.