1629-33-0

Usage

Uses

Used in Polymer Synthesis:
N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE is used as a crosslinking agent in the synthesis of polymers, resins, and coatings. Its ability to form covalent bonds with other molecules makes it a valuable component in the production of various polymeric materials.
Used in Adhesives:
In the Adhesives Industry, N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE is used as a crosslinking agent for enhancing the adhesive properties of polymers. This improves the bonding strength and durability of adhesive products.
Used in Elastomers:
In the Elastomers Industry, N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE is used as a component in the synthesis of polymers that exhibit elastic properties. Its incorporation into elastomeric materials contributes to their flexibility and resilience.
Used in Coatings:
In the Coatings Industry, N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE is used as a crosslinking agent in the formulation of coatings. This improves the hardness, chemical resistance, and overall performance of the coatings.
Used in Epoxy Resins:
N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE is used in the formulation of epoxy resins, which are widely used in various applications due to their excellent adhesion, mechanical strength, and chemical resistance.
Used in Pharmaceutical Industry:
In the Pharmaceutical Industry, N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE has potential applications as a building block in the synthesis of various drug molecules. Its unique structure and reactivity make it a promising candidate for the development of new pharmaceutical compounds.

InChI:InChI=1/C11H18N2/c1-13(10-8-12)9-7-11-5-3-2-4-6-11/h2-6H,7-10,12H2,1H3

Relevant academic research and scientific papers

Synthesis and pharmacological evaluation of Tic-hydantoin derivatives as selective σ1 ligands. Part 2

Herein is described a new class of selective σ1 ligands consisting of tetrahydroisoquinoline-hydantoin (Tic-hydantoin) derivatives. Compound 1a has high affinity (IC50 = 16 nM) for σ1 receptor and is selective in a large panel of therapeutic targets. This study presents structural changes on the side chain of the Tic-hydantoin core. Analogs of higher affinity could be identified (IC50 ≈ 2-3 nM).

N-(amino)alkyl)-1-pyrrolidine, 1-piperidine and 1-homopiperidinecarboxamides (and thiocarboxamides) with sulfur linked substitution in the 2, 3 or 4-positions

Novel pyrrolidine, piperidine and homopiperidinecarboxamide and thiocarboxamide compounds having the formula: STR1 wherein X is --S--, --S(O)-- or --S(O)2 --; A is a loweralkalene chain and A1 and A2 are alkalene chains when p and d are one; R, R1 and R2 are hydrogen, loweralkyl, phenyl cycloalkyl or phenylalkyl and R1 and R2 may form a heterocyclic residue with the adjacent nitrogen atom; Q is a selected aromatic radical, and the pharmaceutically acceptable acid addition salts useful as cardiac antiarrhythmia agents are disclosed. Novel chemical intermediates, unsubstituted on pyrrolidine, piperidine and homopiperidine nitrogen but with --(A2)p --X--(A2)d --Q side chain are also disclosed.

N-[(amino)alkyl]-1-pyrrolidine, 1-piperidine and 1-homopiperidinecarboxamides (and thiocarboxamides) with sulfur linked substitution in the 2, 3 or 4-position

Novel pyrrolidine, piperidine and homopiperidinecarboxamide and thiocarboxamide compounds having the formula: STR1 wherein X is --S--, --S(O)-- or --S(O)2 --; A is a loweralkalene chain and A1 and A2 are alkalene chains when p and d are one; R, R1 and R2 are hydrogen, loweralkyl, phenyl cycloalkyl or phenylalkyl and R1 and R2 may form a heterocyclic residue with the adjacent nitrogen atom; Q is a selected aromatic radical, and the pharmaceutically acceptable acid addition salts useful as cardiac antiarrhythmia agents are disclosed. Novel chemical intermediates, unsubstituted on pyrrolidine, piperidine and homopiperidine nitrogen but with --(A2)p --X--(A2)d --Q side chain are also disclosed.