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:2576-47-8
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inquiryUnique advantages for 2-Bromoethylamine hydrobromide Cas2576-47-8 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White to light beige crystalline powder Package:25kg/dru
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inquiryProduct Name: 2-Bromoethylamine hydrobromide Synonyms: 2-bromoethanaminehydrobromide;2-bromo-ethanaminhydrobromide;2-bromo-ethylaminhydrobromide;beta-bromoethylaminehydrobromide;bromoethylamine,hydrobromide;2-Bromoethylazanium bromide;2-Bromoethyl
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inquiryName: 2-Bromoethylamine hydrobromide CAS:2576-47-8 MF: C8H16N2 Appearance:White Powder Storage:Store in cool and dry place, away from sun light. Package:25KG Application:Cosmetic Raw Materials, Detergent Raw Materials, Hair Care Chemicals Transport
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inquiry2-Bromoethylamine hydrobromideAppearance:Pls see the Details Storage:Keep away of light, hot, water, Store in dry, dark and ventilated place Package:according to customers' requirements Application:Steroids, Cosmetics Ingredients, APIs, Intermediates
Superior quality moderate price & quick delivery Appearance:slight yellow to white crystalline powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request
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inquiryProduct Name: 2-Bromoethylamine hydrobromide Synonyms: 2-bromoethanaminehydrobromide;2-bromo-ethanaminhydrobromide;2-bromo-ethylaminhydrobromide;beta-bromoethylaminehydrobromide;bromoethylamine,hydrobromide;2-bromo-2-ethylamine hydrobromide;2-
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Min.Order:1 Gram
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inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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inquiryConditions | Yield |
---|---|
With hydrogen bromide In 5,5-dimethyl-1,3-cyclohexadiene at 0 - 10℃; for 12h; | 99% |
With hydrogen bromide at 0℃; dann auf 170grad Erhitzen; | |
With hydrogen bromide Darstellung; | |
With hydrogen bromide |
Conditions | Yield |
---|---|
In chloroform at 20°C, pptn.; discussion of mechanism;; | 89% |
In chloroform at 20°C, pptn.; discussion of mechanism;; | 89% |
Conditions | Yield |
---|---|
With hydrogen bromide |
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid at 170℃; |
2-bromoethylamine hydrobromide
Conditions | Yield |
---|---|
With hydrogen bromide |
2-bromoethylamine hydrobromide
1-amino-2-azidoethane
Conditions | Yield |
---|---|
With sodium azide In water at 80℃; for 16h; | 100% |
With sodium azide In water at 75℃; | 93% |
With sodium azide; sodium hydroxide In water | 92% |
dibutoxythiophosphoryl isothiocyanate
2-bromoethylamine hydrobromide
2-<(dibutoxyphosphinothioyl)imino>thiazolidine
Conditions | Yield |
---|---|
With triethylamine In benzene at 60 - 65℃; for 8h; | 100% |
With triethylamine In benzene at 60℃; for 8h; Addition; cyclization; | 91% |
di-tert-butyl dicarbonate
2-bromoethylamine hydrobromide
2-(tert-butoxycarbonylamino)ethyl bromide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 18h; | 100% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 1h; | 100% |
With sodium hydrogencarbonate In tetrahydrofuran; water at 20℃; for 6h; | 100% |
2,6-diisopropylbenzenamine
2-bromoethylamine hydrobromide
N1-(2,6-diisopropylphenyl)ethane-1,2-diamine
Conditions | Yield |
---|---|
Stage #1: 2,6-diisopropylbenzenamine; 2-bromoethylamine hydrobromide for 96h; Reflux; Stage #2: With sodium hydroxide In diethyl ether | 100% |
In toluene for 18h; Heating; | 74% |
In toluene at 110℃; for 18h; | 70% |
In toluene at 100℃; for 48h; | 40% |
With sodium hydroxide In toluene at 110℃; for 12h; |
3-[(4-methylphenyl)sulfonyl]imidazo[1,2-d]-1,2,4-thiadiazole
2-bromoethylamine hydrobromide
N-(2-Bromoethyl)imidazo[1,2-d][1,2,4]thiadiazol-3-amine
Conditions | Yield |
---|---|
100% |
2-bromoethylamine hydrobromide
(+)-3-(4-nitrophenoxycarbonyl)-4S-(3,4-difluorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid methyl ester
Conditions | Yield |
---|---|
With sodium hydroxide; potassium carbonate In tetrahydrofuran; water | 100% |
With sodium hydroxide; potassium carbonate In tetrahydrofuran; water | 100% |
2-bromoethylamine hydrobromide
Conditions | Yield |
---|---|
Stage #1: trans-10-allyloxy-9-oxo-3-thia-5,8,10-triazatricyclo[6.2.1.02,6]undeca-2(6),4-diene-7-carboxylic acid With 4-methyl-morpholine In tetrahydrofuran at -50℃; for 0.25h; Inert atmosphere; Stage #2: With pivaloyl chloride In tetrahydrofuran at -50℃; for 1h; Inert atmosphere; Stage #3: 2-bromoethylamine hydrobromide In tetrahydrofuran at -30℃; for 2h; Inert atmosphere; | 100% |
2-bromoethylamine hydrobromide
Conditions | Yield |
---|---|
Stage #1: trans-10-allyloxy-9-oxo-3-thia-5,8,10-triazatricyclo[6.2.1.02,6]undeca-2(6),4-diene-7-carboxylic acid With 4-methyl-morpholine In tetrahydrofuran at -50℃; for 0.25h; Inert atmosphere; Stage #2: 2-bromoethylamine hydrobromide With pivaloyl chloride at -50 - -30℃; for 3h; | 100% |
2-bromoethylamine hydrobromide
benzyl chloroformate
benzyl N-(2-bromoethyl)carbamate
Conditions | Yield |
---|---|
With sodium hydrogencarbonate Ambient temperature; | 99% |
With sodium hydroxide In 1,4-dioxane; water at 0 - 20℃; for 13.33h; Inert atmosphere; | 99% |
With sodium hydroxide In 1,4-dioxane; water at 0 - 20℃; for 13.3333h; Inert atmosphere; | 99% |
2-bromoethylamine hydrobromide
4-chlorobenzenesulfonyl chloride
2-(4-chlorobenzenesulfonylamino)ethyl bromide
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; | 99% |
With triethylamine In dichloromethane for 0.0833333h; ice-cooling; | 96% |
With triethylamine In dichloromethane at 0℃; for 0.333333h; Inert atmosphere; | 87% |
2-bromoethylamine hydrobromide
diphenylphosphane
(2-aminoethyl)diphenylphosphane
Conditions | Yield |
---|---|
With cesium hydroxide; 4 Angstroem MS In N,N-dimethyl-formamide at 23℃; for 23h; | 99% |
With cesium hydroxide; 4 A molecular sieve In N,N-dimethyl-formamide at 23℃; for 23h; | 99% |
Stage #1: diphenylphosphane With potassium tert-butylate In tetrahydrofuran for 1h; Inert atmosphere; Schlenk technique; Glovebox; Stage #2: 2-bromoethylamine hydrobromide In tetrahydrofuran at 20℃; Inert atmosphere; Schlenk technique; Glovebox; | 38% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 48h; Inert atmosphere; | 99% |
Stage #1: 2-bromoethylamine hydrobromide With sodium ethanolate In ethanol for 0.0833333h; Stage #2: thiophenol In ethanol at 20℃; for 13h; Reflux; | 81% |
Stage #1: 2-bromoethylamine hydrobromide With sodium ethanolate In ethanol for 0.0833333h; Stage #2: thiophenol In ethanol at 20℃; for 13h; Reflux; | 81% |
2-bromoethylamine hydrobromide
benzenesulfonyl chloride
N-(2-bromo-ethyl)-benzenesulfonamide
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane for 1.5h; Cooling with ice; | 98% |
With N-ethyl-N,N-diisopropylamine In dichloromethane for 1.5h; Cooling with ice; | 98% |
With triethylamine In dichloromethane at 0℃; for 0.333333h; Inert atmosphere; | 80% |
With sodium carbonate In water at 20℃; for 16h; | 66% |
With water; sodium carbonate |
2-bromoethylamine hydrobromide
5-bromo-4-chloroquinazoline
10-bromo-2,3-dihydroimidazo<1,2-c>quinazoline
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In tetrahydrofuran for 66h; Ambient temperature; | 98% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 4h; | 98% |
2-bromoethylamine hydrobromide
2′-O-(4-nitrophenoxycarbonyl)-3′,5′-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine
Conditions | Yield |
---|---|
With pyridine; triethylamine at 20℃; for 4h; Inert atmosphere; | 98% |
O,O-dipropyl phosphoroisothiocyanatidothioate
2-bromoethylamine hydrobromide
2-<(dipropoxyphosphinothioyl)imino>thiazolidine
Conditions | Yield |
---|---|
With triethylamine In benzene at 60 - 65℃; for 8h; | 97.5% |
With triethylamine In benzene at 60℃; for 8h; Addition; cyclization; | 97% |
Cholesteryl chloroformate
2-bromoethylamine hydrobromide
C30H50BrNO2
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at -4 - 20℃; for 16h; Cooling with ice; | 97.4% |
With triethylamine In dichloromethane at 20℃; for 16h; Cooling with ice; | 97.4% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 16h; Cooling with ice; | 97.4% |
2-bromoethylamine hydrobromide
2,4,6-trimethylaniline
N-(2,4,6-trimethylphenyl)-1,2-diaminoethane
Conditions | Yield |
---|---|
Stage #1: 2-bromoethylamine hydrobromide; 2,4,6-trimethylaniline In water for 95h; Stage #2: With potassium hydroxide In dichloromethane | 97% |
In toluene for 23h; Reflux; | 89% |
In toluene for 0.666667h; Heating; | 86% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 4h; | 97% |
bis(2-aminoethanethiolato)nickel(II)
2-bromoethylamine hydrobromide
Conditions | Yield |
---|---|
With triethyl amine In N,N-dimethyl-formamide a suspn. of Ni-complex in DMF was heated to 85°C, BrC2H4NH2*HBr was added as a solid followed immediately by N(C2H5)3, the mixt. was heated at 85°C for a addn. 15 min; filtered, washed with diethyl ether, and air dried; | 97% |
2-nitro-4-(trifluoromethyl)benzenesulfonyl chloride
2-bromoethylamine hydrobromide
N-(2-bromoethyl)-2-nitro-4-(trifluoromethyl)benzenesulfonamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 25℃; for 16h; Inert atmosphere; | 97% |
2-bromoethylamine hydrobromide
N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-N'-(2-bromoethyl)-3,4,5,6-tetrahydrophthalamide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile | 96.4% |
dipropyl phosphorisothiocyanatidate
2-bromoethylamine hydrobromide
Thiazolidin-(2E)-ylidene-phosphoramidic acid dipropyl ester
Conditions | Yield |
---|---|
With triethylamine In benzene at 60℃; for 14h; | 96% |
With triethylamine In benzene at 60℃; for 8h; Addition; cyclization; | 96% |
2-bromoethylamine hydrobromide
1-Adamantanecarbonyl chloride
N-(2-Bromoethyl)adamantane-1-carboxamide
Conditions | Yield |
---|---|
In xylene for 7h; Heating; | 96% |
2-bromoethylamine hydrobromide
4-bromophenyl isoselenocyanate
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 4h; | 96% |
2-bromoethylamine hydrobromide
2-Nitrobenzenesulfonyl chloride
N-(2-bromoethyl)-2-nitrobenzenesulfonamide
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 1h; Inert atmosphere; | 96% |
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 1h; | 82% |
With potassium carbonate In acetonitrile at 20 - 60℃; for 2h; | 73% |
3-nitrothiobenzamide
2-bromoethylamine hydrobromide
2-(3-nitrophenyl)-4,5-dihydro-1,3-thiazole
Conditions | Yield |
---|---|
Stage #1: 3-nitrothiobenzamide; 2-bromoethylamine hydrobromide In water at 60 - 70℃; for 4h; Stage #2: With sodium carbonate In water | 96% |
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