| Identification | More | [Name]
1-Benzyl-2-methyl-1H-imidazole | [CAS]
13750-62-4 | [Synonyms]
1-BENZYL-2-METHYLIMIDAZOLE
LABOTEST-BB LT00455538
N-BENZYL-2-METHYLIMIDAZOLE
2-methyl-1-(phenylmethyl)-1h-imidazol
2-methyl-1-(phenylmethyl)-1H-Imidazole
Imidazole, 1-benzyl-2-methyl-
1-benzyl-2-methyl-1H-imidazole
1-BENZYL-2-METHYLIMIDAZOLE, TECH., 90%
1H-Imidazole, 2-methyl-1-(phenylmethyl)-
2-Methyl-N-benzylimidazole
Curezol-1B2MZ
Epicure-BM-112
2-Methyl-1-benzyl-1H-imidazole | [EINECS(EC#)]
237-333-8 | [Molecular Formula]
C11H12N2 | [MDL Number]
MFCD00010637 | [Molecular Weight]
172.23 | [MOL File]
13750-62-4.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
NI7722500
| [HS Code ]
29332900 |
| Hazard Information | Back Directory | [Chemical Properties]
clear light yellow to amber liquid | [Uses]
1-Benzyl-2-methylimidazole may be employed as catalyst to investigate the effect of catalysts on the curing reaction of the biphenyl epoxy (4,4′-diglycidyloxy-3,3′,5,5′-tetramethyl biphenyl)dicyclopentadiene type phenolic resin system. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 71, p. 383, 1949 DOI: 10.1021/ja01170a002 | [General Description]
1-Benzyl-2-methylimidazole is a nitrogen heterocycle and forms mixed ligand Pt(II) complexes. 1-Benzyl-2-methylimidazole on treatement with ammonia and sodium yields 2-methylimidazole. Deposition of plasma-polymerized 1-benzyl-2-methylimidazole (PPBMI) thin films onto glass substrates by glow discharge technique have been reported. | [Synthesis]
A suspension of 10 mmol of 2-methyl-1H-imidazole was formed with 10 mmol of potassium carbonate in 10 mL of acetonitrile and stirred at room temperature for 15 minutes. Subsequently, 10 mmol of benzyl chloride was added to the reaction system and the reaction mixture was heated to 70 °C and stirred continuously for 72 hours. Upon completion of the reaction, the solvent was removed by rotary evaporation and the residue was dissolved in 20 mL of ethyl acetate and washed with deionized water (2 x 10 mL). The organic phase was concentrated under reduced pressure and purified by silica gel column chromatography (eluent: chloroform) to afford the target compound 1-benzyl-2-methylimidazole in 38% yield. The product was a yellow oil; UV-Vis (chloroform, λmax/nm): 290; IR (KBr, ν/cm-1): 2939, 1712, 1508, 1434, 1365, 1272, 1118, 983, 721; 1H NMR (250.13 MHz, CDCl3) δ: 7.43-7.32 (m, 5H). 7.17-7.14 (m, 2H), 6.99 (d, J=1.3 Hz, 1H), 6.84 (d, J=1.2 Hz, 1H), 5.11 (s, 2H), 2.27 (s, 3H); 13C NMR (62.9 MHz, CDCl3) δ: 144.3, 138.0, 129.3, 128.1, 127.5, 127.1, 120.9, 49.2, 13.4. | [References]
[1] Asian Journal of Chemistry, 2014, vol. 26, # 8, p. 2381 - 2388
[2] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 22, p. 6495 - 6499
[3] Journal of Structural Chemistry, 2016, vol. 57, # 4, p. 835 - 839
[4] Zh. Strukt. Kim., 2016, vol. 57, # 4, p. 873 - 876,4
[5] Patent: US4560690, 1985, A |
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