886505-22-2

Basic information

• Product Name: [(1-Methyl-1H-imidazol-2-yl)methyl]-(tetrahydrofuran-2-ylmethyl)amine dihydrochloride
• Synonyms: [(1-Methyl-1H-imidazol-2-yl)methyl]-(tetrahydrofuran-2-ylmethyl)amine dihydrochloride;N-[(1-methylimidazol-2-yl)methyl]-1-(oxolan-2-yl)methanamine
• CAS NO: 886505-22-2
• Molecular Formula: C10H19Cl2N3O
• Molecular Weight: 268.18336
• Mol File: 886505-22-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [(1-Methyl-1H-imidazol-2-yl)methyl]-(tetrahydrofuran-2-ylmethyl)amine dihydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: [(1-Methyl-1H-imidazol-2-yl)methyl]-(tetrahydrofuran-2-ylmethyl)amine dihydrochloride(886505-22-2)
• EPA Substance Registry System: [(1-Methyl-1H-imidazol-2-yl)methyl]-(tetrahydrofuran-2-ylmethyl)amine dihydrochloride(886505-22-2)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 886505-22-2(Hazardous Substances Data)

Upstream product

• 4795-29-3 TETRAHYDROFURFURYLAMINE 
• 13750-81-7 N-methyl-2-imidazolcarboxaldehyde 

Relevant articles and documents

Iron(III) complexes of N2O and N3O donor ligands as functional models for catechol dioxygenase enzymes: Ether oxygen coordination tunes the regioselectivity and reactivity

A series of mononuclear iron(iii) complexes of the type [Fe(L)Cl 3], where L is a systematically modified N2O or N 3O ligand with a methoxyethyl/tetrahydrofuryl ether oxygen donor atom, have been isolated and studied as models for catechol dioxygenases. The X-ray crystal structures of [Fe(L2)Cl3] 2, [Fe(L6)Cl3] 6, [Fe(L5)(TCC)Cl] 5a, where H2TCC = tetrachlorocatechol, [Fe(L6)(TCC)Br] 6a, and the μ-oxo dimer [{Fe(L6)Cl}2O](ClO 4)26b have been successfully determined. In [Fe(L2)Cl 3] 2 the N2O ligand is facially coordinated to iron(iii) through the pyridine and secondary amine nitrogen atoms and the tetrahydrofuryl oxygen atom. In [Fe(L6)Cl3] 6, [Fe(L5)(TCC)Cl] 5a and [Fe(L6)(TCC)Br] 6a the N3O donor ligands L5 and L6 act as a tridentate N3 donor ligand coordinated through two pyridine and one secondary amine nitrogen atoms, whereas the ether oxygen is not coordinated. The spectral and electrochemical properties of the adducts [Fe(L)(DBC)Cl] of 1-8, where H2DBC = 3,5-di-tert-butylcatechol, in DMF and their solvated adduct species [Fe(L)(DBC)(Sol)]+, where Sol = DMF/H2O, generated in situ in dichloromethane, respectively, have been investigated. The product analysis demonstrates that the adducts [Fe(L)(DBC)Cl] effect cleavage of catechol in the presence of O2 in DMF to give mainly the intradiol (I) product with a small amount of the extradiol (E) product (E/I, 0.2:1-0.7:1). Interestingly, the solvated species [Fe(L)(DBC)(Sol)]+ derived from 1-4 cleave H2DBC to provide mainly the extradiol cleavage products with lower amounts of intradiol products (E/I, 2.3:1-4.3:1) in dichloromethane. In contrast, the solvated species [Fe(L)(DBC)(Sol)]+ derived from 5-8 cleave H2DBC to provide both extradiol and intradiol products (E/I, 0.6:1-2.3:1) due to the involvement of the ether oxygen donor of the methoxyethyl/tetrahydrofuryl arm in the coordination to iron(iii) upon removal of a chloride ion. The Royal Society of Chemistry 2011.