Best reputation and rich experience Professional R&D team Best quality under ISO9000:2015 Customized products with all documents Modern smart processing Fast delivery date Free samples available Appearance:Liquid Storage:Store at room temperature
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Cas:925-90-6
Min.Order:1 Kilogram
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Min.Order:1 Metric Ton
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Type:Manufacturers
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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
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Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
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Min.Order:1 Milliliter
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Min.Order:1 Kilogram
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Type:Trading Company
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Min.Order:1 Metric Ton
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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Cas:925-90-6
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inquiryEthylmagnesium bromide CAS:925-90-6 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 organic inte
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Min.Order:1 Gram
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryHangzhou Fandachem Co.,Ltd is leading exporter of Grignard Reagent, Ethylmagnesium bromide 1.0M,2 .0M, 3.0M solution in THF, bromoethylmagnesium, ethvlmagnesiumbromide, CAS: 925-90-6 in China, we supply other Grignard Reagent also: methylmagnesium
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Min.Order:1 Liter
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Type:Other
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Min.Order:0 Metric Ton
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ProName: High quality Ethylmagnesium Bromide su... CasNo: 925-90-6 Molecular Formula: C2H5BrMg Appearance: white-off solid or colorless liquid ( ... Application: organic intermediates DeliveryTime: Instock PackAge: 25kgs/fiber drum or 200kgs/
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Min.Order:1 Metric Ton
FOB Price: $3.0 / 6.0
Type:Trading Company
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Min.Order:10 Gram
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryConditions | Yield |
---|---|
With magnesium In tetrahydrofuran at 18℃; for 0.125h; Inert atmosphere; Flow reactor; | 98% |
With magnesium In diethyl ether at 25℃; under 5171.62 Torr; Solvent; Concentration; Inert atmosphere; Flow reactor; | 96% |
With magnesium In diethyl ether at 26.9℃; Mechanism; Thermodynamic data; Eact, various solvents; |
Conditions | Yield |
---|---|
With magnesium In tetrahydrofuran at 20℃; for 4h; Inert atmosphere; | 83% |
pentaethyldigermane
di-tert-butyl peroxide
A
tetraethyldigermane
B
((CH3CH2)2Ge)4
C
ethylmagnesium bromide
D
octaethyltrigermane
Conditions | Yield |
---|---|
In benzene Irradiation (UV/VIS); digermane soln. irradiating in the presence of an excess of t-Bu2O2; product content detd. by high-pressure chromy.; | A 34% B 3% C 11% D 26% |
Conditions | Yield |
---|---|
In diethyl ether Et4BMgBr*4THF in ether stirred at 25°C for 6 h; not isolated; detected by NMR; | A 20% B 20% |
ethyl bromide
9,10-dihydro-9,10-anthracendiyl-tris(THF)magnesium
A
9-ethyl-9,10-dihydroanthracene
B
9,10-diethyl-9,10-dihydro-anthracene
C
1,2-Diaethyl-1,2-dihydro-anthracen
D
ethylmagnesium bromide
E
2-ethyl-1,2-dihydroanthracene
F
1,4-Diethyl-1,4-dihydro-anthracene
Conditions | Yield |
---|---|
In toluene for 1h; Ambient temperature; other primary, secondary and tertiary alkyl, aryl, allyl, propargyl and benzyl halides; other solvents, other molar ratios RX/1; other temperatures; other reaction times; |
ethyl bromide
9,10-dihydro-9,10-anthracendiyl-tris(THF)magnesium
A
9-ethyl-9,10-dihydroanthracene
B
9,10-diethyl-9,10-dihydro-anthracene
C
ethylmagnesium bromide
D
2-ethyl-1,2-dihydroanthracene
Conditions | Yield |
---|---|
In diethyl ether for 16h; Ambient temperature; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
ethyl bromide
A
9-ethyl-9,10-dihydroanthracene
B
9,10-diethyl-9,10-dihydro-anthracene
C
ethylmagnesium bromide
D
2-ethyl-1,2-dihydroanthracene
Conditions | Yield |
---|---|
With magnesium anthracene * 3 THF In toluene for 1h; Ambient temperature; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
diethyl ether
triethyllead bromide
A
ethylmagnesium bromide
B
tetraethyllead(IV)
diethyl ether
triethyllead bromide
A
ethylmagnesium bromide
B
tetraethyllead(IV)
Conditions | Yield |
---|---|
In diethyl ether at 20 - 30℃; |
Conditions | Yield |
---|---|
With iodine; magnesium In diethyl ether Inert atmosphere; |
Conditions | Yield |
---|---|
With diethyl ether |
m-bromobenzoic aldehyde
ethylmagnesium bromide
(+/-)-1-(3-bromophenyl)propanol
Conditions | Yield |
---|---|
In diethyl ether at -78 - 20℃; | 100% |
In diethyl ether | 92% |
Stage #1: m-bromobenzoic aldehyde; ethylmagnesium bromide In diethyl ether for 1.08333h; Cooling with ice; Stage #2: With hydrogenchloride In diethyl ether; water | 88% |
Conditions | Yield |
---|---|
With methylaluminum bis(2,6-di-tert-butylphenoxide) In diethyl ether; toluene at -78℃; for 2h; | 100% |
In diethyl ether at 0 - 20℃; | 87% |
Stage #1: ethylmagnesium bromide; benzaldehyde In tetrahydrofuran at 30℃; for 24h; Inert atmosphere; Stage #2: With water In tetrahydrofuran Inert atmosphere; | 73% |
Conditions | Yield |
---|---|
With methylaluminum bis(2,6-di-tert-butylphenoxide) In diethyl ether; toluene at -78℃; for 2h; | 100% |
In diethyl ether at 0 - 20℃; | 90% |
In diethyl ether; benzene | |
In diethyl ether |
4-Trifluoromethylbenzaldehyde
ethylmagnesium bromide
(+/-)-1-<4-(trifluoromethyl)phenyl>-1-propanol
Conditions | Yield |
---|---|
In tetrahydrofuran for 2h; Ambient temperature; | 100% |
In diethyl ether for 2h; Ambient temperature; | 93.7% |
In diethyl ether Ambient temperature; | 89% |
2-formylbenzo[b]furan
ethylmagnesium bromide
1-(benzofuran-2-yl)propan-1-ol
Conditions | Yield |
---|---|
In tetrahydrofuran; diethyl ether at 20℃; for 4h; Inert atmosphere; | 100% |
In tetrahydrofuran; diethyl ether at -20℃; for 2h; |
ethylmagnesium bromide
3,4-dihydro-6-methoxy-1-(4-methoxyphenyl)-2-naphthalenecarboxaldehyde
1-<6-methoxy-1-(p-methoxyphenyl)-3,4-dihydro-2-naphthalenyl>propan-1-ol
Conditions | Yield |
---|---|
In diethyl ether 1.) overnight, 2.) reflux, 2 h; | 100% |
ethylmagnesium bromide
5-Bromo-1,1-dimethyl-1H-indene
1,1-dimethyl-5-ethylind-2-ene
Conditions | Yield |
---|---|
With 1,2-bis(diphenylphosphino)ethane nickel(II) chloride In diethyl ether for 16h; Heating; | 100% |
ethylmagnesium bromide
2-(pentafluorophenyl)-4,4-dimethyl-2-oxazoline
Conditions | Yield |
---|---|
In benzene Heating; | 100% |
ethylmagnesium bromide
Conditions | Yield |
---|---|
In tetrahydrofuran at -93℃; | 100% |
ethylmagnesium bromide
(2S,6R)-2-benzyloxymethoxy-7-(4-methoxybenzyloxy)-6-methoxyethoxymethoxyheptan-3-one
(2S,3R,6R)-2-benzyloxymethoxy-3-ethyl-7-(4-methoxybenzyloxy)-6-methoxyethoxymethoxyheptan-3-ol
Conditions | Yield |
---|---|
In tetrahydrofuran at -78℃; for 2h; | 100% |
In tetrahydrofuran at -78℃; for 1.5h; Yield given; |
ethylmagnesium bromide
6-hydroxy-7-methyl-1-(phenylsulfinyl)spirononane-3,2'-<1,3>dioxolane>-9-one
9-ethyl-6,9-dihydroxy-7-methyl-1-(phenylsulfinyl)-spirononane-3,2'-<1,3>dioxolane>
Conditions | Yield |
---|---|
With chloro-trimethyl-silane In tetrahydrofuran; diethyl ether at -78℃; for 0.25h; | 100% |
ethylmagnesium bromide
(2R,5S)-5-benzyloxy-2-<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>heptan-4-one
(2R,4R,5S)-5-Benzyloxy-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4-ethyl-heptan-4-ol
Conditions | Yield |
---|---|
In tetrahydrofuran at -78℃; | 100% |
ethylmagnesium bromide
(2S,6S)-2-benzyloxymethoxy-6,7-isopropylidenedioxyheptan-3-one
(2S,3R,6S)-2-benzyloxymethoxy-3-ethyl-6,7-isopropylidenedioxyheptan-3-ol
Conditions | Yield |
---|---|
In tetrahydrofuran at -93℃; for 2h; | 100% |
ethylmagnesium bromide
Conditions | Yield |
---|---|
In tetrahydrofuran at -78℃; | 100% |
96% |
ethylmagnesium bromide
2-(F-phenyl)-4,4,6-trimethyl-5,6-dihydro-4H-oxazine
Conditions | Yield |
---|---|
In benzene for 10h; Heating; | 100% |
ethylmagnesium bromide
6-methoxy-1-(p-methoxyphenyl)-1,2,3,4-tetrahydro-2-naphthaldehyde
1-<6-methoxy-1-(p-methoxyphenyl)-1,2,3,4-tetrahydro-2-naphthalenyl>propan-1-ol
Conditions | Yield |
---|---|
In diethyl ether 1.) overnight, 2.) reflux, 2 h; | 100% |
ethylmagnesium bromide
ethyl-2-(dimethylphenylsilyl)pent-4-enoate
4-(dimethylphenylsilyl)hept-6-en-3-one
Conditions | Yield |
---|---|
In tetrahydrofuran for 3h; Heating; | 100% |
In tetrahydrofuran for 3h; Heating; |
Conditions | Yield |
---|---|
In tetrahydrofuran for 3h; Heating; | 100% |
In tetrahydrofuran for 3h; Heating; |
ethylmagnesium bromide
(S)-N-methoxy-N-methyl-3-triisopropylsilanyloxy-2-methylpropionamide
(S)-1-triisopropylsilanyloxy-2-methyl-3-pentanone
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1.5h; | 100% |
In tetrahydrofuran at 0 - 20℃; for 2h; | 89% |
ethylmagnesium bromide
ortho-bromobenzaldehyde
1-(2-bromophenyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: ethylmagnesium bromide; ortho-bromobenzaldehyde In tetrahydrofuran at -70 - 20℃; for 6h; Stage #2: With water; ammonium chloride In tetrahydrofuran | 100% |
In diethyl ether at 0 - 20℃; | 95% |
In tetrahydrofuran; diethyl ether at -78 - 0℃; Inert atmosphere; | 81% |
ethylmagnesium bromide
6H-benzo[c]thiochromen-6-one
10-Ethyl-10H-9-thia-phenanthren-10-ol
Conditions | Yield |
---|---|
In tetrahydrofuran for 0.5h; Heating; | 100% |
ethylmagnesium bromide
(S)-2-[(4R,5S,6S)-2,2-Di-tert-butyl-6-((S)-1-[1,3]dithiolan-2-yl-ethyl)-5-methyl-[1,3,2]dioxasilinan-4-yl]-propionaldehyde
(R)-2-[(4S,5S,6S)-2,2-Di-tert-butyl-6-((S)-1-[1,3]dithiolan-2-yl-ethyl)-5-methyl-[1,3,2]dioxasilinan-4-yl]-pentan-3-ol
Conditions | Yield |
---|---|
In diethyl ether at -78℃; for 2.5h; | 100% |
ethylmagnesium bromide
(3aS,7R,7aS)-7-Methoxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-one
3-[(R)-((4S,5S)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-methoxy-methyl]-pentan-3-ol
Conditions | Yield |
---|---|
In tetrahydrofuran at 0℃; Alkylation; | 100% |
ethylmagnesium bromide
N-methoxy-N-methyl-4-(1H-pyrrol-1-yl)butanamide
6-(1H-pyrrol-1-yl)hexan-6-one
Conditions | Yield |
---|---|
In diethyl ether at 18℃; for 2h; | 100% |
Stage #1: ethylmagnesium bromide; N-methoxy-N-methyl-4-(1H-pyrrol-1-yl)butanamide In diethyl ether at 18℃; for 1h; Stage #2: With potassium hydrogensulfate In diethyl ether at -40℃; for 0.1h; Further stages.; | 95% |
In diethyl ether at 18℃; for 1h; Grignard reaction; | |
In tetrahydrofuran at 0 - 20℃; for 2.5h; Inert atmosphere; Schlenk technique; | |
In diethyl ether at 0℃; for 1h; Inert atmosphere; Sealed tube; | 7.09 g |
ethylmagnesium bromide
(E)-2-methyl-1,3-diphenyl-2-(p-tolylsulfinyl)aziridine
Conditions | Yield |
---|---|
In tetrahydrofuran at -78 - 20℃; Metallation; | 100% |
ethylmagnesium bromide
5-tert-butyldimethylsilyloxypentanal
Conditions | Yield |
---|---|
100% | |
Stage #1: ethylmagnesium bromide; 5-tert-butyldimethylsilyloxypentanal In diethyl ether at 0℃; for 0.5h; Inert atmosphere; Stage #2: With hydrogenchloride In diethyl ether; water Inert atmosphere; | |
In tetrahydrofuran at 0℃; for 0.5h; Inert atmosphere; |
5-bromo-3,4-dihydro-2H-pyran
ethylmagnesium bromide
5-ethyl-3,4-dihydropyran
Conditions | Yield |
---|---|
With 1,2-bis(diphenylphosphino)ethane nickel(II) chloride In tetrahydrofuran | 100% |
ethylmagnesium bromide
2,2'-(2,3-dimethoxy-1,4-phenylene)bis(4,4-dimethyl-2-oxazoline)
2,2'-(2,3-diethyl-1,4-phenylene)bis(4,4-dimethyl-2-oxazoline)
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 2h; | 100% |
In tetrahydrofuran; water | 1.98 g (100%) |
ethylmagnesium bromide
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 22℃; | 100% |
ethylmagnesium bromide
2-((tert-butyl(diphenyl)silyl)oxy)acetic acid ethyl ester
Conditions | Yield |
---|---|
Stage #1: ethylmagnesium bromide; 2-((tert-butyl(diphenyl)silyl)oxy)acetic acid ethyl ester With titanium(IV) isopropylate In tetrahydrofuran at 20℃; for 12h; Stage #2: With ammonium chloride In tetrahydrofuran | 100% |
Stage #1: ethylmagnesium bromide; 2-((tert-butyl(diphenyl)silyl)oxy)acetic acid ethyl ester With titanium(IV) isopropylate In tetrahydrofuran at 20℃; Stage #2: With water In tetrahydrofuran | 97% |
With titanium(IV) isopropylate In tetrahydrofuran at -10 - 25℃; for 5h; Kulinkovich cyclopropanation; | 80% |
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