1629-33-0

Basic information

• Product Name: N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE
• Synonyms: N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE;N-methyl-N-(2-phenylethyl)ethane-1,2-diamine(SALTDATA: FREE)
• CAS NO: 1629-33-0
• Molecular Formula: C₁₁H₁₈N₂
• Molecular Weight: 178.27
• Mol File: 1629-33-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 265.2°C at 760 mmHg
• Flash Point: 106°C
• Appearance: /
• Density: 0.975g/cm³
• Vapor Pressure: 0.0093mmHg at 25°C
• Refractive Index: 1.535
• CAS DataBase Reference: N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE(1629-33-0)
• EPA Substance Registry System: N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE(1629-33-0)

Safety Data

• Hazardous Substances Data: 1629-33-0(Hazardous Substances Data)

Usage

General Description

N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE is a chemical compound with the formula C11H18N2. It is a diamine derivative with a methyl group and a 2-phenylethyl group attached to the nitrogen atoms. N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE is commonly used as a crosslinking agent in the synthesis of polymers, resins, and coatings. It has been employed in the production of polymers used in adhesives, elastomers, and coatings, as well as in the formulation of epoxy resins. Additionally, it has potential applications in the pharmaceutical industry, particularly as a building block in the synthesis of various drug molecules. Due to its unique structure and reactivity, N-METHYL-N-(2-PHENYLETHYL)ETHANE-1,2-DIAMINE is a versatile chemical with a wide range of industrial and pharmaceutical applications.

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 articles and documents

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-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.