330205
5-Chloro-1-methylimidazole
98%
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About This Item
Empirical Formula (Hill Notation):
C4H5ClN2
CAS Number:
Molecular Weight:
116.55
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-827-6
MDL number:
Product Name
5-Chloro-1-methylimidazole, 98%
InChI key
NYDGOZPYEABERA-UHFFFAOYSA-N
InChI
1S/C4H5ClN2/c1-7-3-6-2-4(7)5/h2-3H,1H3
SMILES string
Cn1cncc1Cl
assay
98%
form
liquid
refractive index
n20/D 1.511 (lit.)
bp
82-85 °C/11 mmHg (lit.)
density
1.25 g/mL at 25 °C (lit.)
functional group
chloro
Quality Level
Application
5-Chloro-1-methylimidazole was used in synthesis of C-5 functionalized N-methylated imidazoles.
General description
5-Chloro-1-methylimidazole is a 5-halo-1-methylimidazole. It participates in electron-rich iron(III) porphyrin complex catalyzed epoxidation of olefins.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
204.8 °F - closed cup
flash_point_c
96 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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An efficient route to 5-iodo-1-methylimidazole: synthesis of xestomanzamine A.
Panosyan FB and Still IWJ.
Canadian Journal of Chemistry, 79(7), 1110-1114 (2001)
W Nam et al.
Journal of inorganic biochemistry, 80(3-4), 219-225 (2000-09-23)
An electron-rich iron(III) porphyrin complex (meso-tetramesitylporphinato)iron(III) chloride [Fe(TMP)Cl], was found to catalyze the epoxidation of olefins by aqueous 30% H2O2 when the reaction was carried out in the presence of 5-chloro-1-methylimidazole (5-Cl-1-Melm) in aprotic solvent. Epoxides were the predominant products
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