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:693-05-0
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Cas:693-05-0
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inquiryProduct Name: 3-Methylaminopropionitrile Synonyms: (2-Cyanoethyl)methyl amine;(2-cyanoethyl)methylamine;(Methylamino)propionitrile;3-(methylamino)-propanenitril;3-(Methylamino)propanenitrile;3-(methylamino)-propionitril;3-(n-methylamin
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiry3-Methylaminopropionitrile CAS:693-05-0 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
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Min.Order:1 Gram
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Min.Order:10 Gram
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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Cas:693-05-0
Min.Order:1 Gram
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Type:Lab/Research institutions
inquirySuperior quality, moderate price & quick delivery. Appearance:CLEAR YELLOW LIQUID Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:as per your request Application:Used as Pharmaceutical Intermediates,ect. Trans
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Min.Order:100 Gram
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Conditions | Yield |
---|---|
With C12H18NO3S(1+)*HO4S(1-) at 25℃; for 0.0666667h; Ionic liquid; Neat (no solvent); chemoselective reaction; | 99% |
In methanol a) 0 deg C, 1 h, b) RT, overnight; | 84% |
In ethanol at 15℃; under 760.051 Torr; | 83.5% |
3-methyl-2-oxo-1,3-oxazolidine
N-(2-cyanoethyl)-N-methylamine
Conditions | Yield |
---|---|
With potassium cyanide; 18-crown-6 ether at 100℃; for 8h; Neat (no solvent); | 50% |
Conditions | Yield |
---|---|
unter Kuehlung; | |
unter Kuehlung; |
N-(2-cyanoethyl)-N-methylamine
3-(methylamino)propanamidoxime
Conditions | Yield |
---|---|
With hydroxylamine In ethanol; water at 20 - 50℃; for 27h; | 99.5% |
With hydroxylamine |
N-(2-cyanoethyl)-N-methylamine
1-chloro-2,4-dinitro-benzene
2,4-dinitro-N-methyl-N-β-cyanoethylaniline
Conditions | Yield |
---|---|
at 20℃; for 7h; | 99% |
N-(2-cyanoethyl)-N-methylamine
di-tert-butyl dicarbonate
t-butyl N-(2-cyanoethyl)-N-methylcarbamate
Conditions | Yield |
---|---|
In dichloromethane | 99% |
In dichloromethane at 20℃; for 2h; | 90% |
In dichloromethane at 20℃; for 2h; | 90% |
N-(2-cyanoethyl)-N-methylamine
p-tolyl isoselenocyanate
1-(2-cyanoethyl)-1-methyl-3-(4-tolyl)selenourea
Conditions | Yield |
---|---|
With pyridine In toluene at 20℃; for 24h; Inert atmosphere; | 99% |
N-(2-cyanoethyl)-N-methylamine
[4S-[4α,5β,6β(S*)]]-4-methyl-3-[[[(2-methylpropoxy)carbonyl]oxy]methyl]-7-oxo-6-[1-[(triethylsilyl)oxy]ethyl]-1-azabicyclo[3.2.0]hepten-2-ene-2-carboxylic acid (4-nitrophenyl)methyl ester
Conditions | Yield |
---|---|
With 1,4-di(diphenylphosphino)-butane; tris(dibenzylideneacetone)dipalladium(0) chloroform complex In N,N-dimethyl-formamide at 20℃; for 12 - 36h; | 98% |
N-(2-cyanoethyl)-N-methylamine
p-chlorphenylisocyanate
3-(4-chlorophenyl)-1-(2-cyanoethyl)-1-methylurea
Conditions | Yield |
---|---|
In benzene | 96% |
N-(2-cyanoethyl)-N-methylamine
2,3-epoxy-2-methyl-1-phenylpropan-1-one
2-Hydroxy-2-methyl-3--1-phenyl-1-propanone
Conditions | Yield |
---|---|
In isopropyl alcohol for 15h; Heating; | 96% |
2,4-dichlorothieno[3,2-d]pyrimidine
N-(2-cyanoethyl)-N-methylamine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In ethyl acetate at 20℃; | 95% |
N-(2-cyanoethyl)-N-methylamine
sodium 4-methylbenzenesulfinate
N-(2-cyanoethyl)-N,4-dimethylbenzenesulfonamide
Conditions | Yield |
---|---|
With iodine In water at 20℃; for 3h; Green chemistry; | 93% |
N-(2-cyanoethyl)-N-methylamine
1-nitroanthraquinone
1-(methylamino)anthraquinone
Conditions | Yield |
---|---|
In butan-1-ol at 118℃; for 135h; | 92% |
In methanol at 130℃; for 13h; Rate constant; other solvent; |
N-(2-cyanoethyl)-N-methylamine
2-chloro-6,7-dimethoxyquinazolin-4-amine
N-(4-amino-6,7-dimethoxy-quinazolin-2-yl)-N-methyl-2-cyanoethyl-amine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In butan-1-ol for 3h; Heating / reflux; | 92% |
In i-Amyl alcohol at 135 - 140℃; for 4h; | 78% |
In i-Amyl alcohol |
Conditions | Yield |
---|---|
Stage #1: N-(2-cyanoethyl)-N-methylamine; 3-nitrosalicylic aldehyde In tetrahydrofuran for 0.25h; Stage #2: With sodium diacetoxy(acetyl)boranuide In tetrahydrofuran at 20℃; for 16h; | 92% |
Conditions | Yield |
---|---|
With triethylamine In water; toluene at 20℃; for 1.5h; | 92% |
Conditions | Yield |
---|---|
With sulfuric acid for 3h; Heating; | 91% |
With barium dihydroxide |
2-acetyl-2-methyloxirane
N-(2-cyanoethyl)-N-methylamine
4--3-hydroxy-3-methyl-2-butanone
Conditions | Yield |
---|---|
In isopropyl alcohol for 15h; Heating; | 91% |
Cyclopentanecarboxylic acid chloride
N-(2-cyanoethyl)-N-methylamine
N-(3-cyanopropyl)-N-methylcyclopentanecarboxamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 1h; Ambient temperature; | 91% |
1-chloro-4-methanesulfonyl-2-nitrobenzene
N-(2-cyanoethyl)-N-methylamine
3-[(4-Methanesulfonyl-2-nitro-phenyl)-methyl-amino]-propionitrile
Conditions | Yield |
---|---|
In butan-1-ol at 118℃; for 2h; | 91% |
N-(2-cyanoethyl)-N-methylamine
[(((2-5-η)-2,4-pentadienyl)methylamino)propionitrile]tricarbonyliro
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran N2-atmosphere; stirring (-40°C, 20 min, 25°C, 30 min); 50% EtOAc / hexanes addn., washing (H2O, brine), drying (MgSO4), concg.,chromy. (SiO2, 15% EtOAc / hexanes); | 91% |
N-(2-cyanoethyl)-N-methylamine
4-methoxy-2,3,6-trimethylbenzenesulfonyl chloride
N-(2-Cyanoethyl)-4-methoxy-N,2,3,6-tetramethylbenzenesulfonamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; for 16h; | 91% |
N-(2-cyanoethyl)-N-methylamine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 3h; | 91% |
N-(2-cyanoethyl)-N-methylamine
ethyl bromoacetate
[(2-cyanoethyl)methylamino]acetic acid ethyl ester
Conditions | Yield |
---|---|
With potassium carbonate In butanone Heating; | 88.9% |
With potassium carbonate In butanone Heating; |
N-(2-cyanoethyl)-N-methylamine
3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl isocyanate
Conditions | Yield |
---|---|
In diethyl ether for 2h; Ambient temperature; | 88% |
N-(2-cyanoethyl)-N-methylamine
dimedone
3-<2-cyanoethyl(methyl)amino>-5,5-dimethylcyclohex-2-enone
Conditions | Yield |
---|---|
In xylene for 3h; Heating; | 87% |
N-(2-cyanoethyl)-N-methylamine
5'-tosyladenosine
5'-<(2-cyanoethyl)methylamino>-5'-deoxyadenosine
Conditions | Yield |
---|---|
at 20℃; for 120h; | 87% |
at 20℃; for 120h; | 87% |
for 120h; Ambient temperature; | 80% |
for 168h; Ambient temperature; | 42% |
N-(2-cyanoethyl)-N-methylamine
benzoic acid anhydride
N-methyl-N-cyanoethyl benzamide
Conditions | Yield |
---|---|
With sodium hydroxide In dichloromethane | 87% |
Conditions | Yield |
---|---|
With copper(l) iodide; oxygen In 1,2-dichloro-ethane at 100℃; for 24h; Schlenk technique; | 86% |
With copper(l) iodide; oxygen In 1,2-dichloro-ethane at 100℃; for 24h; | 86% |
N-(2-cyanoethyl)-N-methylamine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; | 86% |
N-(2-cyanoethyl)-N-methylamine
4-bromonaphthalene-1,8-dicarboximide
4-N-methylaminonaphthalimide
Conditions | Yield |
---|---|
In methanol at 130℃; Rate constant; Kinetics; Thermodynamic data; sealed tube; other temperature; | 85% |
In methanol at 130℃; for 18h; sealed tube; | 85% |
Conditions | Yield |
---|---|
With pyridine; N-hydroxyphthalimide; oxygen; copper dichloride In N,N-dimethyl-formamide at 30℃; for 2h; chemoselective reaction; | 85% |
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