| Identification | More | [Name]
2-Chloro-1H-imidazole | [CAS]
16265-04-6 | [Synonyms]
2-CHLORO-1H-IMIDAZOLE | [Molecular Formula]
C3H3ClN2 | [MDL Number]
MFCD02179530 | [Molecular Weight]
102.52 | [MOL File]
16265-04-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
165-170 °C
| [Boiling point ]
252.7±23.0 °C(Predicted) | [density ]
1.405±0.06 g/cm3(Predicted) | [storage temp. ]
Keep Cold | [form ]
powder to crystal | [pka]
11.23±0.10(Predicted) | [color ]
White to Almost white | [InChI]
InChI=1S/C3H3ClN2/c4-3-5-1-2-6-3/h1-2H,(H,5,6) | [InChIKey]
OCVXSFKKWXMYPF-UHFFFAOYSA-N | [SMILES]
C1(Cl)NC=CN=1 | [CAS DataBase Reference]
16265-04-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Symbol(GHS) ]
 
GHS05,GHS07 | [Signal word ]
Danger | [Hazard statements ]
H302-H315-H318-H335 | [Precautionary statements ]
P280-P301+P312+P330-P302+P352-P305+P351+P338+P310 | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed.
R37/38:Irritating to respiratory system and skin .
R41:Risk of serious damage to eyes. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/39:Wear suitable protective clothing and eye/face protection . | [WGK Germany ]
3 | [Hazard Note ]
Irritant | [HS Code ]
2933299090 |
| Hazard Information | Back Directory | [Chemical Properties]
2-Chloro-1H-imidazole(16265-04-6) is an imidazole compound with the appearance of white to off-white powder to crystal, molecular weight 102.52, melting point 166.0 ~ 170.0 °C, it is sensitive to heat, and is usually stored at 2-8°C. It can be used as an antimicrobial agent in the manufacture of imidazoles.
| [Uses]
2-Chloroimidazole(16265-04-6) is used in pharmaceuticals, drug candidates, ligands for transition metal catalysts and other molecular functional materials.
| [Definition]
ChEBI: An imidazole compound having a chloro substituent at the 2-position. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 63, p. 12, 1998 DOI: 10.1021/jo970355+ | [Synthesis]
The general procedure for the synthesis of 2-chloroimidazole from 1-(diethoxymethyl)imidazole is as follows: with reference to Example 9, 2-chloroimidazole was prepared as follows: N-(diethoxymethyl)imidazole (50.0 g) was dissolved in tetrahydrofuran (200 ml), and a n-hexane solution of 2.6 M n-butyllithium (120 ml) was added slowly and dropwise to this solution. The addition of tetrahydrofuran solution (100 ml) of hexachloroethane (73.9 g) was continued dropwise at -35°C. The reaction mixture was kept at the same temperature for 5 min, then warmed up to -20°C and 6N hydrochloric acid (100 ml) was added, after which it was restored to room temperature and left to stand for 5 min. The aqueous layer was separated and the organic layer was extracted with 1N hydrochloric acid, the extract was combined with the aqueous layer and washed with ether. This was followed by neutralization with 6N aqueous sodium hydroxide and extraction with ethyl acetate. The organic layer was separated, dried with anhydrous magnesium sulfate and the solvent was removed by distillation to give the crude product. The crude product was ground with dichloromethane to give finally 2-chloroimidazole (26.0 g, yield: 85.0%) as a light brown solid.1H-NMR (CDCl3) δ (ppm): 10.64 (1H, bs), 7.05 (1H, s). | [References]
[1] Patent: EP1553088, 2005, A1. Location in patent: Page/Page column 52 |
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
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Alfa Aesar
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Jia Xing Isenchem Co.,Ltd
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0573-85285100 18627885956 |
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