high quality Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Best price 2-Ethyl-1-butanol 2-Ethyl-1-butanol 97-95-0 in stock Supply 2-Ethyl-1-butanol 97-95-0? Introduction: Synchem is an innovative manufacturer specializing in contract manufacturing to the pharmaceutical, agrochemical and electrical ind
Cas:97-95-0
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inquiry1-Butanol, 2-ethyl-; 2-ethyl-1-butano; 2-ethyl-butan-1-ol; 2-Ethylbutan-1-ol; 2-Ethylbutanol-1; 2-iithylbutanol; 3-Methylolpentane; -Pentyl carbinol CAS No: 97-95-0 Molecular formula: C6H14O Molecular weight: 102.17 2-ethyl-1-butanol
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Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
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Provide 2-Ethyl-1-butanol 97-95-0 manufacturer Molecular Formula:C6H14O Molecular Weight:102.17 CAS :97-95-0 EINECS:202-621-4 Chemical Name 2-Ethyl-1-butanol Synonyms
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inquiry2-ETHYL-1-BUTANOL Basic information Product Name: 2-ETHYL-1-BUTANOL
Cas:97-95-0
Min.Order:100 Gram
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≥99%, stockAppearance:clear colorless to slightly yellowish liquid Package:1kg/bottle;50kg/100kg/drum Application:OLED Transportation:by air, by sea
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Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether at -5 - 5℃; for 3h; Inert atmosphere; | 91.2% |
With ethanol; sodium at 100℃; | |
Hydrogenation; |
Conditions | Yield |
---|---|
With chloroaluminium tetrahydroborate on poly(4-vinylpyridine) In ethanol for 9h; Heating; | 90% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether at -5 - 5℃; for 3h; Inert atmosphere; | 89.2% |
With lithium borohydride In methanol; diethyl ether for 0.5h; Heating; | 87% |
With sodium tetrahydroborate In methanol; tert-butyl alcohol Heating; | 84 % Chromat. |
Conditions | Yield |
---|---|
With hydrogen at 150℃; under 9750.98 Torr; for 4.5h; | 87% |
With poly-η-(pyridine)zinc borohydride In diethyl ether for 1.6h; Ambient temperature; | 80% |
With hexarhodium hexadecacarbonyl; carbon monoxide; aminated polymer; water In benzene at 80℃; under 7600 Torr; for 24h; | 27 % Chromat. |
ethanol
sodium ethanolate
A
octanol
B
2-Ethylhexyl alcohol
C
2-ethyl-1-butanol
D
butan-1-ol
E
hexan-1-ol
Conditions | Yield |
---|---|
With [HN-(CH2CH2PiPr2)2]Mn(CO)2Br at 150℃; for 24h; Temperature; Reagent/catalyst; Guerbet Reaction; Schlenk technique; | A n/a B n/a C n/a D 33% E n/a |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
2-Ethylbutyraldehyde
tert-butylmagnesium chloride
A
4-ethyl-2,2-dimethyl-hexan-3-ol
B
2-ethyl-1-butanol
2-Ethylbutyraldehyde
1,1-dimethylpropylmagnesium chloride
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With diethyl ether |
2-Ethylbutyraldehyde
1,1-dimethylpropylmagnesium chloride
A
2-ethyl-1-butanol
B
5-ethyl-3,3-dimethyl-heptan-4-ol
hexa-1,5-diene-3,4-diol
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With sulfuric acid at 100 - 120℃; Hydrieren des Reaktionsprodukts bis zur Aufnahme von 6 Atomen Wasserstoff; |
diethyl ether
chlorure d'acide ethyl-2 butyrique
tert-butylmagnesium chloride
A
4-ethyl-2,2-dimethyl-hexan-3-ol
B
2-ethyl-1-butanol
diethyl ether
tert-butylmagnesium chloride
A
4-ethyl-2,2-dimethyl-hexan-3-ol
B
2-ethyl-1-butanol
2-ethylbut-3-en-1-ol
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With methanol; palladium Hydrogenation; |
chlorure d'acide ethyl-2 butyrique
1,1-dimethylpropylmagnesium chloride
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With diethyl ether |
chlorure d'acide ethyl-2 butyrique
1,1-dimethylpropylmagnesium chloride
A
2-ethyl-1-butanol
B
5-ethyl-3,3-dimethyl-heptan-4-ol
Conditions | Yield |
---|---|
With diethyl ether |
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With silver(I) nitrite |
Conditions | Yield |
---|---|
With potassium carbonate und Erhitzen des Reaktionsprodukts auf 100grad und anschliessendes Hydrieren an einem Kupfer-Katalysator bei 240grad; |
Conditions | Yield |
---|---|
With aluminum oxide; hydrogen; magnesium oxide; copper(II) oxide at 300℃; | |
With aluminum oxide; hydrogen; magnesium oxide; copper(II) oxide at 300℃; |
2-Ethyl-1-pyrrolidino-1-butene
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate; boron trifluoride diethyl etherate; dihydrogen peroxide 1.) THF, 25 deg C, 3 h, 2.) ether, 25 deg C, 3 h; Yield given. Multistep reaction; |
4-(2-ethylbut-1-en-1-yl)morpholine
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate; boron trifluoride diethyl etherate; dihydrogen peroxide 1.) THF, 25 deg C, 3 h, 2.) ether, 25 deg C, 3 h; Yield given. Multistep reaction; |
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate; boron trifluoride diethyl etherate; dihydrogen peroxide 1.) THF, 25 deg C, 3 h, 2.) ether, 25 deg C, 3 h; Yield given. Multistep reaction; |
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate; boron trifluoride diethyl etherate; dihydrogen peroxide 1.) THF, 25 deg C, 3 h, 2.) ether, 25 deg C, 3 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
at 250℃; under 128714 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
at 250℃; under 102971 - 154457 Torr; Hydrogenation; |
ethyl 2-butylacetoacetate
A
Ethyl hexanoate
B
2-ethyl-1-butanol
C
hexan-1-ol
Conditions | Yield |
---|---|
at 250℃; under 128714 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
at 258℃; |
Conditions | Yield |
---|---|
at 120 - 160℃; under 73550.8 - 147102 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
at 200℃; |
Conditions | Yield |
---|---|
at 200℃; |
2-ethyl-1-butanol
6-bromo-4-chloroquinoline-3-carboxylic acid ethyl ester
Conditions | Yield |
---|---|
Stage #1: 2-ethyl-1-butanol With sodium hydride In tetrahydrofuran at 0℃; for 0.166667h; Inert atmosphere; Stage #2: 6-bromo-4-chloroquinoline-3-carboxylic acid ethyl ester In tetrahydrofuran at 20℃; for 2h; Inert atmosphere; | 100% |
2-ethyl-1-butanol
di(n-butyl)tin oxide
1,1,3,3-tetrabutyl-1,3-bis(2-ethylbutyloxy)distannoxane
Conditions | Yield |
---|---|
at 140℃; under 525.053 Torr; for 1.5h; Product distribution / selectivity; Gas phase; | 99% |
at 157℃; under 487.549 - 760.051 Torr; Industry scale; Inert atmosphere; | 99% |
at 157℃; for 2h; Inert atmosphere; Large scale; | 99% |
In toluene at 130℃; for 3.5h; | 295 g |
In toluene at 130℃; for 0.5h; | 295 g |
2-ethyl-1-butanol
dioctyltin(IV) oxide
1,1,3,3-tetraoctyl-1,3-bis(2-ethylbutyloxy)distannoxane
Conditions | Yield |
---|---|
at 157℃; under 487.549 - 760.051 Torr; Industry scale; Inert atmosphere; | 99% |
at 165℃; under 760.051 Torr; for 0.666667h; Product distribution / selectivity; Industry scale; Inert atmosphere; | 99% |
at 165℃; under 760.051 Torr; for 0.666667h; Product distribution / selectivity; Industry scale; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
dioctyl-bis(2-ethylbutyloxy)tin; 1,1,3,3-tetraoctyl-1,3-bis(2-ethylbutyloxy)distannoxane at 120℃; for 4h; Product distribution / selectivity; Industry scale; Autoclave; | 99% |
dibutyl-bis(2-ethylbutyloxy)tin; 1,1,3,3-tetrabutyl-1,3-bis(2-ethylbutyloxy)distannoxane at 120℃; under 30003 Torr; Product distribution / selectivity; Autoclave; Industry scale; | |
dioctyl-bis(2-ethylbutyloxy)tin; 1,1,3,3-tetraoctyl-1,3-bis(2-ethylbutyloxy)distannoxane at 120℃; for 4h; Product distribution / selectivity; Autoclave; Industry scale; | |
1,1,3,3-tetraoctyl-1,3-bis(2-ethylbutyloxy)distannoxane In water at 120℃; for 220h; Industry scale; Autoclave; |
2-ethyl-1-butanol
Conditions | Yield |
---|---|
Stage #1: methyl 7-hydroxy-8-methyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate; 2-ethyl-1-butanol With triphenylphosphine polystyrene In tetrahydrofuran for 0.25h; Stage #2: With ethyl azodicarboxylate In tetrahydrofuran at 20℃; | 98% |
Conditions | Yield |
---|---|
With trifluoroacetic acid In dichloromethane at 20℃; for 5h; | 98% |
Conditions | Yield |
---|---|
With pyridine; tetrachlorosilane Substitution; | 95% |
With tetrachlorosilane at 250℃; |
2-ethyl-1-butanol
acetoacetic acid methyl ester
2-ethylbutyl 3-oxobutanoate
Conditions | Yield |
---|---|
With m-nitrobenzene boronic acid; toluene for 5h; Heating; Green chemistry; | 95% |
2-ethyl-1-butanol
Conditions | Yield |
---|---|
In dimethylsulfoxide-d6; [D3]acetonitrile at 40℃; for 15h; Inert atmosphere; | 95% |
2-ethyl-1-butanol
2-<(trimethylsilyl)methyl>-1-cyclohexenemethanol
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane; trimethylphosphine(hexafluoroacetylacetone)copper; Selectfluor In N,N,N,N,N,N-hexamethylphosphoric triamide; acetonitrile at 110℃; for 8h; Reagent/catalyst; Solvent; | 94.6% |
2-ethyl-1-butanol
(2-Trimethylsilanylmethyl-cyclopent-1-enyl)-methanol
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane; trimethylphosphine(hexafluoroacetylacetone)copper; Selectfluor In N,N,N,N,N,N-hexamethylphosphoric triamide; acetonitrile at 80℃; for 12h; Reagent/catalyst; Solvent; | 94.4% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In acetonitrile at 60℃; for 15h; | 94% |
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane for 14h; Schlenk technique; Inert atmosphere; | 93% |
N-tert-butoxycarbonyl-L-leucine
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; for 16h; | 93% |
ethyl 7-hydroxy-2-(trifluoromethyl)-2H-chromene-3-carboxylate
2-ethyl-1-butanol
Conditions | Yield |
---|---|
Stage #1: ethyl 7-hydroxy-2-(trifluoromethyl)-2H-chromene-3-carboxylate; 2-ethyl-1-butanol With triphenylphosphine polystyrene In tetrahydrofuran at 20℃; for 0.25h; not specified; Stage #2: With ethyl azodicarboxylate In tetrahydrofuran at 20℃; | 92% |
L-alanin
2-ethyl-1-butanol
toluene-4-sulfonic acid
(S)-2-ethylbutyl 2-aminopropanoate tosylate salt
Conditions | Yield |
---|---|
In toluene for 14h; Reflux; | 91% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene for 14h; Reflux; | 91% |
Conditions | Yield |
---|---|
Stage #1: 2-ethyl-1-butanol; L-<3,3,3-2H3>alanine at 0℃; for 0.0833333h; Stage #2: With thionyl chloride at 60℃; for 6h; | 90.2% |
2-ethyl-1-butanol
3-(iodomethyl)pentane
Conditions | Yield |
---|---|
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 0℃; for 0.5h; Appel Halogenation; | 90% |
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane for 1h; Inert atmosphere; | 89% |
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 1.5h; | 34% |
Conditions | Yield |
---|---|
With rhodium(III) chloride hydrate; potassium carbonate; triphenylphosphine at 140℃; for 24h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With cerium(III) bromide; tetrabutylammomium bromide In acetonitrile for 24h; Reagent/catalyst; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With phosphorus; tetraethylammonium iodide In water; acetonitrile electrolysis; | A 89% B n/a C n/a |
2-ethyl-1-butanol
di(n-butyl)tin oxide
A
dibutyl-bis(2-ethylbutyloxy)tin
B
1,1,3,3-tetrabutyl-1,3-bis(2-ethylbutyloxy)distannoxane
Conditions | Yield |
---|---|
at 140℃; under 450.045 Torr; for 1.5h; Product distribution / selectivity; Gas phase; | A 11% B 88% |
at 120℃; for 6h; |
(3S,4aR,6S,8aR)-6-[2-(1H-Tetrazol-5-yl)-phenylamino]-decahydro-isoquinoline-3-carboxylic acid
2-ethyl-1-butanol
Conditions | Yield |
---|---|
With hydrogenchloride Heating; | 87% |
2-ethyl-1-butanol
bis(2-ethylbutyl)amine
Conditions | Yield |
---|---|
With ammonium carbonate In 5,5-dimethyl-1,3-cyclohexadiene for 24h; Inert atmosphere; Sealed tube; Reflux; | 87% |
2-ethyl-1-butanol
N-tert-butoxycarbonyl-L-phenylalanine
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 0 - 20℃; for 16h; | 87% |
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