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Cas:13551-86-5
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryfactory?direct?sale Application:Fine chemical intermediates, used as the main raw material for the synthesis of various pesticides, medicines, surfactants, polymer monomers, and antifungal agents
Cas:13551-86-5
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiry1-chloro-3-(2-nitro-1H-imidazol-1-yl)propan-2-one
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol at 0℃; | 97% |
2-nitro-1H-imidazole
epichlorohydrin
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
Conditions | Yield |
---|---|
With potassium carbonate for 0.25 - 0.333333h; Heating / reflux; | 83% |
With potassium carbonate for 0.333333h; Reflux; | |
With potassium carbonate In acetone Heating / reflux; |
potassium phtalimide
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
2-(2-hydroxy-3-(2-nitro-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 85℃; for 2h; | 87% |
4-(1,2-dicarba-closo-dodecaboran(12)-1-yl)phenyl isocyanate
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
1-(chloromethyl)-2-(2-nitroimidazoly)ethyl N-(4-(1,2-dicarba-closo-dodecaboran(12)-1-yl)phenyl)carbamate
Conditions | Yield |
---|---|
In toluene refluxed for 24 h; evapd., the residue is recrystd. (chloroform); | 81% |
4-amino-1-butyne hydrochloride
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
1-but-3-ynylamino-3-(2-nitro-imidazol-1-yl)-propan-2-ol
Conditions | Yield |
---|---|
With potassium carbonate In methanol for 5h; Heating / reflux; | 70% |
piperidine
pyrographite
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
Pimonidazole
Conditions | Yield |
---|---|
In methanol; ethanol; water | 65% |
2-(2-(2-aminoethoxy)ethoxy)ethan-1-ol
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
C12H22N4O6
Conditions | Yield |
---|---|
With potassium carbonate In methanol for 14h; Heating / reflux; | 65% |
closo-1,2-caboranylethyl-1-(4-amino)butane
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
1-[4-(closo-1,2-decaboranylethyl)-butylamino]-3-(2-nitro-imidazol-1-yl)-propan-2-ol
Conditions | Yield |
---|---|
With triethylamine In ethanol for 5h; Heating / reflux; | 52% |
1,2-dicarba-closo-dodecaborane-1-carboxylic acid
trimethylsilylazide
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
1-(chloromethyl)-2-(2-nitroimidazol-1-yl)ethyl N-(1,2-dicarba-closo-dodecaboran(12)-1-yl)carbamate
Conditions | Yield |
---|---|
With thionyl chloride In N,N-dimethyl-formamide; toluene the carboranecarboxylic acid is boiled under reflux with thionyl chloride and DMF for 4 h, evapd., the residue is dissolved in toluene and treated with azidotrimethylsilane, refluxed for 18 h, cooled, the alcohol isadded, refluxed for 1 h; evapd., the residue is dissolved in chloroform, cooled to 0°C, elem. anal.; | 38% |
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
2-nitro-1-(2-oxiranylmethyl)-1H-imidazole
Conditions | Yield |
---|---|
With 18-crown-6 ether In acetonitrile | |
In ethyl acetate at 20℃; for 1h; | 300 mg |
With sodium hydroxide In water; ethyl acetate at 20℃; for 1h; |
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: ethyl acetate / 1 h / 20 °C 2.1: ethanol / 0.33 h / 120 °C / Microwave irradiation 2.2: 4 h / 40 °C View Scheme |
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: ethyl acetate / 1 h / 20 °C 2.1: ethanol / 0.33 h / 120 °C / Microwave irradiation 2.2: 4 h / 40 °C 3.1: triethylamine / dichloromethane; ethanol / 0.25 h / 80 °C / Microwave irradiation View Scheme |
α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
1-(2-hydroxy-3-(N'-1,1,1,3,3,3-hexafluoroisopropylpiperazino))-2-nitroimidazole
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium hydroxide / water; ethyl acetate / 1 h / 20 °C 2: sodium hydroxide / acetone / Heating / reflux View Scheme |
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