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

General 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, which is used as a ligand in the synthesis of coordination compounds. This chemical is widely used in coordination chemistry for the synthesis of metal complexes in various industrial and research applications. It is a water-soluble compound and has a variety of potential uses in pharmaceuticals, agrochemicals, and other chemical industries. N,N'-Dicyclohexyl-1,2-ethanediamine Hydrate is an important reagent for various chemical processes and is commonly used as a chelating agent in the formation of coordination complexes.

Upstream product

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

Downstream Products

• 753502-41-9 N-cyclohexyl-N-(2-cyclohexylamino-ethyl)-formamide 
• 4483-46-9 N,N'-dicyclohexyl-N,N'-ethanediyl-bis-formamide 
• 200068-65-1 1,3-dicyclohexyl-imidazolidine 
• 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 
• 61797-62-4 Undec-10-enoic acid cyclohexyl-[2-(cyclohexyl-undec-10-enoyl-amino)-ethyl]-amide 
• 61797-63-5 Decanoic acid cyclohexyl-[2-(cyclohexyl-decanoyl-amino)-ethyl]-amide 
• 61797-68-0 5-Oxo-5-phenyl-pentanoic acid cyclohexyl-{2-[cyclohexyl-(5-oxo-5-phenyl-pentanoyl)-amino]-ethyl}-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 

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.