4013-98-3

Basic information

• Product Name: N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate
• Synonyms: N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate;N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate
• CAS NO: 4013-98-3
• Molecular Formula: C₁₄H₂₈N₂
• Molecular Weight: 242.4008
• EINECS: -0
• Mol File: 4013-98-3.mol
• Article Data: 12

Chemical Properties

• Melting Point: 95 °C
• Boiling Point: 312°C(lit.)
• Appearance: /
• Solubility: soluble in Methanol
• CAS DataBase Reference: N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate(4013-98-3)
• EPA Substance Registry System: N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate(4013-98-3)

Safety Data

• RIDADR: UN 3259 8/PG II
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 4013-98-3(Hazardous Substances Data)

Usage

Description

N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate is a chemical compound with the molecular formula C16H32N2 ? H2O. It is a hydrate form of N,N'-Dicyclohexyl-1,2-ethanediamine, characterized by its water solubility and versatile applications in coordination chemistry. N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate serves as a ligand in the synthesis of coordination compounds, playing a crucial role in the formation of metal complexes for various industrial and research applications.

Uses

Used in Coordination Chemistry:
N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate is used as a ligand for the synthesis of metal complexes, contributing to the development of coordination compounds with potential applications in various fields.
Used in Pharmaceutical Industry:
N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate is used as a chelating agent in the formation of coordination complexes, which can have therapeutic applications or be utilized in drug delivery systems to enhance the efficacy and bioavailability of pharmaceutical compounds.
Used in Agrochemical Industry:
In the agrochemical sector, N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate is employed as a component in the synthesis of metal complexes that can be used in the development of pesticides, fertilizers, or other agrochemical products to improve crop yield and protection.
Used in Chemical Industry:
N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate is utilized as an important reagent in various chemical processes, including the synthesis of catalysts, dyes, and other specialty chemicals, where its chelating properties can enhance the performance and selectivity of these processes.

Upstream product

• 3673-06-1 N,N'-dicyclohexylethylenediimine 
• 107-15-3 ethylenediamine 
• 108-93-0 cyclohexanol 
• 28227-38-5 (N,N'-dicyclohexyl)-1,2-ethanediimine 
• 108-94-1 cyclohexanone 
• 108-91-8 cyclohexylamine 
• 106-93-4 ethylene dibromide 
• 107-06-2 1,2-dichloro-ethane 
• 6780-13-8 1,2-ethanediamine monohydrate 

Downstream Products

• 63632-91-7 (Z)-Undec-9-enoic acid cyclohexyl-{2-[cyclohexyl-((Z)-undec-9-enoyl)-amino]-ethyl}-amide 
• 61797-65-7 N-Cyclohexyl-N-{2-[cyclohexyl-(2-ethyl-butyryl)-amino]-ethyl}-2-ethyl-butyramide 
• 61797-66-8 N-Cyclohexyl-N-{2-[cyclohexyl-(2-octylsulfanyl-acetyl)-amino]-ethyl}-2-octylsulfanyl-acetamide 
• 61797-69-1 6-(4-tert-Butyl-phenylsulfanyl)-hexanoic acid (2-{[6-(4-tert-butyl-phenylsulfanyl)-hexanoyl]-cyclohexyl-amino}-ethyl)-cyclohexyl-amide 
• 865411-26-3 N,N'-dicyclohexylethane-1,2-diamine salt of 7β-[2-(2-amino-4-thiazolyl)-2-((Z)-hydroxyimino)acetamido]-3-vinyl-3-cephem-4-carboxylic acid 
• 52040-05-8 1,3-dicyclohexylimidazolidin-2-one 
• 1428904-89-5 1,1 ,3,3-tetracyclohexyl-2,2-bi-1,3,2-diazaphospholidine 
• 109305-55-7 B,B'-bis(1,3-dicyclohexyl-1,3,2-diazaborolidin-2-yl) 
• 30826-84-7 1,4-dicyclohexyl-imidazolidine-2-thione 

Relevant articles and documents

Diazaphospholene Precatalysts for Imine and Conjugate Reductions

The first examples of 1,3,2-diazaphospholene-catalyzed imine reduction and conjugate reduction reactions are reported. This approach employs readily synthesized alkoxydiazaphospholene precatalysts that can be handled in open air. Reduction of substrates containing Lewis basic functionality, isolated unsaturation, and protic functional groups was accomplished. The synthetic utility of this approach is demonstrated by the synthesis of the important antiparkinson medicine rasagiline and the natural product zingerone.

N-alkylation of ethylenediamine with alcohols catalyzed by CuO-NiO/γ-Al2O3

A simple method for N-alkylation of 1, 2-diaminoethane with different alcohols in a fixed-bed reactor using cheap CuO-NiO/γ-Al2O 3 as the catalyst has been developed. The present catalytic system was applicable in the N-alkylation of 1, 2-diaminoethane with both primary and secondary alcohols. Mono-N-alkylation of 1, 2-diaminoethane with low-carbon alcohols resulted in high yields; the yields of tetra-N-alkylation of 1, 2-diaminoethane with low-carbon alcohols declined markedly with the increase of the molecular volume of alcohols.

Effect of ligand substituents in olefin polymerisation by half-sandwich titanium complexes containing monoanionic iminoimidazolidide ligands-MAO catalyst systems

Various half-sandwich titanium complexes containing iminoimidazolidide ligands, CpTiCl2[1,3-R2(CH2N)2CN] (1a-d) [R = Ph (a), 2,6-Me2C6H3 (b), cyclohexyl (c), tBu (d)], have been employed as the catalyst precursors for ethylene polymerisation, syndiospecific styrene polymerisation, and copolymerisation of ethylene with 1-hexene in the presence of MAO cocatalyst; 1d showed the highest catalytic activity for ethylene polymerisation whereas 1b showed the highest activity for syndiospecific styrene polymerisation.