DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:112-50-5
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Min.Order:1 Gram
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Min.Order:1
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Min.Order:1 Kilogram
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Min.Order:10 Kilogram
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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inquiryTriethylene glycol monoethyl ether CAS:112-50-5 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality
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Min.Order:1 Gram
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Min.Order:1 Kilogram
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inquiryTriethylene glycol monoethyl ether Basic information Product Name: Triethylene glycol monoethyl ether Synonyms: TRI(ETHYLENE GLYCOL) MONOETHYL ETHER, T&;Ethanol, 2-2-(2-ethoxyethoxy)ethoxy-;3,6,9-TRIOXA-1-UNDECANOL;ETHANOL,2-[2-(2-ETHOXYET
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Min.Order:1 Gram
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2-(2-(2-(2-iodoethoxy)ethoxy)ethoxy)ethanol
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
With tri(2-furyl)germane; 2,2’-azobis(4-methoxy-2,4-dimethyl)valeronitrile In water at 80℃; for 1h; | 97% |
ethyl iodide
2,2'-[1,2-ethanediylbis(oxy)]bisethanol
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
With potassium hydroxide In tetrahydrofuran for 4h; Ambient temperature; | 60% |
Conditions | Yield |
---|---|
With sulfuric acid at 80 - 100℃; |
Conditions | Yield |
---|---|
With ethanolamine at 50 - 60℃; |
oxirane
ethoxyethoxyethanol
A
monoethyl ether of triethylene glycol
B
3,6,9,12-tetraoxatetradecan-1-ol
Conditions | Yield |
---|---|
With ethanolamine at 50 - 60℃; |
oxirane
ethoxyethoxyethanol
ethanolamine
A
monoethyl ether of triethylene glycol
B
3,6,9,12-tetraoxatetradecan-1-ol
Conditions | Yield |
---|---|
at 50 - 63℃; |
ethoxyethoxyethanol
2-chloro-ethanol
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
at 70 - 80℃; reagiert das Natriumsalz; |
ethyl bromide
2,2'-[1,2-ethanediylbis(oxy)]bisethanol
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
(i) Na, (ii) /BRN= 1209224/; Multistep reaction; |
Conditions | Yield |
---|---|
at 70 - 80℃; |
Conditions | Yield |
---|---|
With sodium ethanolate |
monoethyl ether of triethylene glycol
p-toluenesulfonyl chloride
2-(2-(2-ethoxyethoxy)ethoxy)ethyl 4-methylbenzenesulfonate
Conditions | Yield |
---|---|
With triethylamine at 0 - 20℃; | 100% |
Stage #1: monoethyl ether of triethylene glycol; p-toluenesulfonyl chloride With dmap In dichloromethane at 20℃; Stage #2: With triethylamine In dichloromethane at 20℃; | 100% |
With pyridine at 0 - 20℃; for 2h; Tosylation; | 97% |
hydrogenchloride
monoethyl ether of triethylene glycol
p-toluenesulfonyl chloride
2-(2-(2-ethoxyethoxy)ethoxy)ethyl 4-methylbenzenesulfonate
Conditions | Yield |
---|---|
Stage #1: monoethyl ether of triethylene glycol; p-toluenesulfonyl chloride With pyridine In diethyl ether for 3.5h; Cooling with ice; Stage #2: hydrogenchloride In water; ethyl acetate | 100% |
Conditions | Yield |
---|---|
With sodium borohydrid In 5,5-dimethyl-1,3-cyclohexadiene | 99% |
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
With 1% Pd on activated carbon; hydrogen In methanol at 20℃; under 2585.81 Torr; for 24h; | 97% |
Multi-step reaction with 3 steps 1.1: dmap / dichloromethane / 20 °C 1.2: 20 °C 2.1: N,N-dimethyl-formamide / 18 h / 80 °C 3.1: hydrazine hydrate / ethanol / 3 h / 76 °C View Scheme | |
Multi-step reaction with 3 steps 1: sodium hydroxide / tetrahydrofuran; water / 2.25 h / 0 - 20 °C / Inert atmosphere 2: N,N-dimethyl-formamide / 3 h / 110 °C / Inert atmosphere 3: hydrazine hydrate / ethanol / 110 °C / Inert atmosphere View Scheme | |
Multi-step reaction with 3 steps 1: sodium hydroxide / tetrahydrofuran; water / 4 h / 0 - 20 °C 2: N,N-dimethyl-formamide / 16 h / Heating 3: hydrazine hydrate / ethanol / 16 h / 110 °C View Scheme | |
Multi-step reaction with 3 steps 1.1: sodium hydroxide / tetrahydrofuran; water / 0.25 h / 0 - 20 °C 1.2: 16 h / 0 - 20 °C 2.1: N,N-dimethyl-formamide / 16 h / 20 - 110 °C 3.1: hydrazine hydrate / ethanol / 16 h / 110 °C View Scheme |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at -10 - 20℃; for 8h; | 95% |
monoethyl ether of triethylene glycol
ethyl acrylate
ethyl 4,7,10,13-tetroxapentadecanoate
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol; toluene for 48h; Addition; Heating; | 94% |
Conditions | Yield |
---|---|
With sodium methylate at 60℃; for 0.166667h; | 92% |
Conditions | Yield |
---|---|
With thionyl chloride at 50℃; for 5h; | 90% |
monoethyl ether of triethylene glycol
2-[2-(2-ethoxyethoxy)ethoxy]ethyl chloride
Conditions | Yield |
---|---|
With thionyl chloride; N,N-dimethyl-formamide | 89% |
With thionyl chloride In toluene at 90℃; for 24h; | 57% |
monoethyl ether of triethylene glycol
3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine
tri(ethylene glycol) ethyl[3-(pyrid-3-yl)-1,2,5-thiadiazol-4-yl]ether
Conditions | Yield |
---|---|
Stage #1: monoethyl ether of triethylene glycol With sodium hydride In tetrahydrofuran Heating; Stage #2: 3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine In tetrahydrofuran Heating; | 88.4% |
Conditions | Yield |
---|---|
With N,N'-dimethylaminopyridine; di-tert-butyl dicarbonate In nitromethane at 50℃; for 16h; | 88% |
Conditions | Yield |
---|---|
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In water at 30 - 45℃; | 88% |
monoethyl ether of triethylene glycol
2-allyloxy-1,2-oxaborolane
2-(2-ethoxy-2-ethoxy-2-ethoxyethoxy)-1,2-oxaborolane
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: allyl alcohol; N2 atmosphere; stirring and heating (160-180°C, 2 h); distn. of allyl alcohol (atmospheric pressure), distn. (vac.); elem. anal.; | 86.7% |
monoethyl ether of triethylene glycol
3-(tert-butyldimethylsilyloxy)glutaric anhydride
C19H38O8Si
Conditions | Yield |
---|---|
In toluene for 16h; Reflux; | 81% |
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane Inert atmosphere; | 80% |
4,4'-dibromo-2,2'-bipyridine
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide for 2h; Inert atmosphere; Reflux; | 77% |
monoethyl ether of triethylene glycol
2,7-dinitro-9H-fluorene-4-carbonyl chloride
2,7-dinitrofluorene-4-carboxylic acid (triethylene glycol monoethyl ether) ester
Conditions | Yield |
---|---|
at 90 - 100℃; for 0.0833333h; | 73% |
monoethyl ether of triethylene glycol
1,3-Diiodobenzene
1,3-bis(2-(2-(2-ethoxyethoxy)ethoxy)ethoxy)benzene
Conditions | Yield |
---|---|
With copper(l) iodide; 1,10-Phenanthroline; caesium carbonate In 5,5-dimethyl-1,3-cyclohexadiene for 20h; Reflux; Inert atmosphere; | 71% |
Conditions | Yield |
---|---|
With zinc(II) acetylacetonate at 0℃; for 18h; Molecular sieve; Sealed tube; Inert atmosphere; | 71% |
monoethyl ether of triethylene glycol
bromoacetic acid
3,6,9,12-Tetraoxatetradecansaeure
Conditions | Yield |
---|---|
With sodium hydride; potassium iodide In tetrahydrofuran at 0 - 5℃; for 12.5h; Inert atmosphere; | 70% |
monoethyl ether of triethylene glycol
N-t-butoxycarbonyl-S-acetamidomethyl-L-cysteine
Conditions | Yield |
---|---|
With dmap In dichloromethane at 0 - 20℃; for 12h; Inert atmosphere; | 67% |
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
aluminum nickel | 66% |
Conditions | Yield |
---|---|
With copper(l) iodide; 1,10-Phenanthroline; caesium carbonate In 5,5-dimethyl-1,3-cyclohexadiene for 20h; Reflux; Inert atmosphere; | 61% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran | 60% |
monoethyl ether of triethylene glycol
Conditions | Yield |
---|---|
for 3h; Reflux; | 57.5% |
Conditions | Yield |
---|---|
With triethylamine for 1h; | 57% |
monoethyl ether of triethylene glycol
cis-norbornene-endo-2,3-dicarboxylic acid
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; | 57% |
monoethyl ether of triethylene glycol
1-bromo-2-(2-(2-ethoxyethoxy)ethoxy)ethane
Conditions | Yield |
---|---|
With carbon tetrabromide; triphenylphosphine In dichloromethane for 16h; Ambient temperature; | 54% |
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