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Shandong Mopai Biotechnology Co., LTD

Shandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W

alpha-(Chloromethyl)-2-nitroimidazole-1-ethanol

Cas:13551-86-5

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

Antimex Chemical Limied

factory?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

alpha-(Chloromethyl)-2-nitroimidazole-1-ethanol

Cas:13551-86-5

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Synthetic route

1-chloro-3-(2-nitro-1H-imidazol-1-yl)propan-2-one
21787-94-0

1-chloro-3-(2-nitro-1H-imidazol-1-yl)propan-2-one

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

Conditions
ConditionsYield
With sodium tetrahydroborate In methanol at 0℃;97%
2-nitro-1H-imidazole
527-73-1

2-nitro-1H-imidazole

epichlorohydrin
106-89-8

epichlorohydrin

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

Conditions
ConditionsYield
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
1074-82-4

potassium phtalimide

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

2-(2-hydroxy-3-(2-nitro-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione
93272-45-8

2-(2-hydroxy-3-(2-nitro-1H-imidazol-1-yl)propyl)isoindoline-1,3-dione

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 85℃; for 2h;87%
4-(1,2-dicarba-closo-dodecaboran(12)-1-yl)phenyl isocyanate
158565-51-6

4-(1,2-dicarba-closo-dodecaboran(12)-1-yl)phenyl isocyanate

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

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
158565-52-7

1-(chloromethyl)-2-(2-nitroimidazoly)ethyl N-(4-(1,2-dicarba-closo-dodecaboran(12)-1-yl)phenyl)carbamate

Conditions
ConditionsYield
In toluene refluxed for 24 h; evapd., the residue is recrystd. (chloroform);81%
4-amino-1-butyne hydrochloride
88211-50-1

4-amino-1-butyne hydrochloride

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

1-but-3-ynylamino-3-(2-nitro-imidazol-1-yl)-propan-2-ol
1021880-41-0

1-but-3-ynylamino-3-(2-nitro-imidazol-1-yl)-propan-2-ol

Conditions
ConditionsYield
With potassium carbonate In methanol for 5h; Heating / reflux;70%
piperidine
110-89-4

piperidine

pyrographite
7440-44-0

pyrographite

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

Pimonidazole
70132-50-2

Pimonidazole

Conditions
ConditionsYield
In methanol; ethanol; water65%
2-(2-(2-aminoethoxy)ethoxy)ethan-1-ol
6338-55-2

2-(2-(2-aminoethoxy)ethoxy)ethan-1-ol

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

C12H22N4O6
1021880-48-7

C12H22N4O6

Conditions
ConditionsYield
With potassium carbonate In methanol for 14h; Heating / reflux;65%
closo-1,2-caboranylethyl-1-(4-amino)butane
1021880-46-5

closo-1,2-caboranylethyl-1-(4-amino)butane

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

1-[4-(closo-1,2-decaboranylethyl)-butylamino]-3-(2-nitro-imidazol-1-yl)-propan-2-ol
1021880-43-2

1-[4-(closo-1,2-decaboranylethyl)-butylamino]-3-(2-nitro-imidazol-1-yl)-propan-2-ol

Conditions
ConditionsYield
With triethylamine In ethanol for 5h; Heating / reflux;52%
1,2-dicarba-closo-dodecaborane-1-carboxylic acid
18178-04-6

1,2-dicarba-closo-dodecaborane-1-carboxylic acid

trimethylsilylazide
4648-54-8

trimethylsilylazide

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol
13551-86-5

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
158565-48-1

1-(chloromethyl)-2-(2-nitroimidazol-1-yl)ethyl N-(1,2-dicarba-closo-dodecaboran(12)-1-yl)carbamate

Conditions
ConditionsYield
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
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

2-nitro-1-(2-oxiranylmethyl)-1H-imidazole
13551-90-1

2-nitro-1-(2-oxiranylmethyl)-1H-imidazole

Conditions
ConditionsYield
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
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

1-(4-(aminomethyl)piperidin-1-yl)-3-(2-nitro-1H-imidazol-1-yl)-propan-2-ol

1-(4-(aminomethyl)piperidin-1-yl)-3-(2-nitro-1H-imidazol-1-yl)-propan-2-ol

Conditions
ConditionsYield
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
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

C33H32N6O8S

C33H32N6O8S

Conditions
ConditionsYield
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
13551-86-5

α-(chloromethyl)-2-nitro-1H-imidazole-1-ethanol

1-(2-hydroxy-3-(N'-1,1,1,3,3,3-hexafluoroisopropylpiperazino))-2-nitroimidazole
1016952-59-2

1-(2-hydroxy-3-(N'-1,1,1,3,3,3-hexafluoroisopropylpiperazino))-2-nitroimidazole

Conditions
ConditionsYield
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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