22811-14-9

Basic information

• Product Name: 2-heptyl-4,5-dihydro-1H-imidazole
• CAS NO: 22811-14-9
• Molecular Formula: C₁₀H₂₀N₂
• Molecular Weight: 168.2792
• Mol File: 22811-14-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 291.7°C at 760 mmHg
• Flash Point: 130.2°C
• Density: 0.96g/cm³
• Vapor Pressure: 0.00334mmHg at 25°C
• Refractive Index: 1.511
• CAS DataBase Reference: 2-heptyl-4,5-dihydro-1H-imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-heptyl-4,5-dihydro-1H-imidazole(22811-14-9)
• EPA Substance Registry System: 2-heptyl-4,5-dihydro-1H-imidazole(22811-14-9)

Safety Data

• Hazardous Substances Data: 22811-14-9(Hazardous Substances Data)

Upstream product

• 54977-31-0 N-(2-amino-ethyl)-octanamide 
• 124-12-9 caprylnitrile 
• 124-13-0 Octanal 
• 107-15-3 ethylenediamine 
• 13831-12-4 octanedithioic acid ethyl ester 
• 17832-30-3 N,N'-dioctanoylethane-1,2-diamine 

Relevant articles and documents

Facile preparation of 2-imidazolines from aldehydes with tert-butyl hypochlorite

An efficient and high-yield preparation of 2-imidazolines was achieved from aldehydes and ethylenediamines in the presence of tert-butyl hypochlorite. By this method, 1,3-bis(imidazolin-2-yl)benzene and 2,6-bis(imidazolin-2-yl) pyridine, which act as chiral ligands, could be prepared directly from the corresponding dialdehydes in high yields. Georg Thieme Verlag Stuttgart.

Compositions and method comprising heterocyclic compounds containing two heteroatoms

A method and compositions for topically administering physiologically active agents through the skin and mucous membranes of humans and animals in a transdermal device or formulation for systemic use or to the skin of humans and animals for localized use comprising applying to such skin or membrane a mixture of said physiologically active agent and a non-toxic, effective penetrating amount of penetration enhancing compound having the structural formula I: STR1 wherein: R is a saturated or unsaturated hydrocarbon group with from 5 to 19 carbon atoms; R' and R" are hydrogen, lower alkyl, trifluoromethyl, lower hydroxyalkyl or lower alkyl ester of lower hydroxyalkyl, with the proviso that both R' and R" are not lower hydroxyalkyl; X is O or NR1 ; R1 being hydrogen, lower alkyl, lower alkenyl, lower hydroxyalkyl or lower alkyl ester of lower hydroxyalkyl are disclosed.