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Cas:765-30-0
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inquiryItems Standard Result Appearance Colorless to transparent liquid Colorless to transparent liquid Water
Cas:765-30-0
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inquiryProduct Description Product website: http://www.finerchem.com Product Name Aminocyclopropane CAS No. 765-30-0 Appearance
Cas:765-30-0
Min.Order:1 Gram
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inquiryBuy Cyclopropylamine CPA CAS 765-30-0 , a chemical intermediate for Cyclopropylamine from TNJ Chemical, China leading Cyclopropylamine suppliers, factory & manufacturers. If you want to buy Cyclopropylamine or buy Erythritol, please mail to sal
Cas:765-30-0
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inquiryCyclopropylamine CPA CAS 765-30-0 is a colorless and transparent liquid with volatility and ammonia smell. It is miscible with water and solvents such as methanol, ethanol, benzene and toluene. Cyclopropylamine is an intermediate of the herbicide c
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inquiry1.Product Discription of 765-30-0 Product Name: Cyclopropylamine Synonyms: Cyclopropanamine;CYCLOPROPYLAMINE;AURORA KA-2551;AKOS BBS-00003593;AMINOCYCLOPROPANE;AMINOTRIMETHYLENE;Cyloprolylamine;Cyclopropyl amine(CPA) Molecular Formula: C3H7
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Min.Order:1 Kilogram
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inquiryCyclopropylamine CAS:765-30-0 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 intermedi
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Min.Order:1 Gram
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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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inquiryHangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting Cyclopropylamine (CPA) cas 765-30-0;Please contact us by email freely. We are leading exporter in China. If you really need this
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Min.Order:0 Metric Ton
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Min.Order:1 Gram
Negotiable
Type:Other
inquirynitrocyclopropane
Cyclopropylamine
Conditions | Yield |
---|---|
With triethylamine In water at 80℃; for 6h; Inert atmosphere; Green chemistry; chemoselective reaction; | 91% |
With hydrogenchloride; iron | |
With methanol; nickel Hydrogenation; |
Conditions | Yield |
---|---|
With sodium hydroxide; sodium hypochlorite; water at 31 - 103℃; Conversion of starting material; Hofmann Rearrangement; Heating / reflux; | 62% |
With bromine dann man behandelt mit Kalilauge und destilliert mit Wasserdampf; | |
zur Bildung; |
Methyl N-cyclopropylcarbamate
Cyclopropylamine
Conditions | Yield |
---|---|
With potassium hydroxide |
Cyclopropylamine
Conditions | Yield |
---|---|
With 1,2-dimethoxyethane; trifluoroacetic anhydride und anschliessend mit KOH in wss. Aethylenglykol; |
Conditions | Yield |
---|---|
With hydrogen azide; chloroform; sulfuric acid |
Cyclopropylamine
Conditions | Yield |
---|---|
With sodium bis(2-methoxyethoxy)aluminium dihydride In toluene at 140℃; for 4h; |
[(1-Ethoxycyclopropyl)oxy]trimethylsilane
Cyclopropylamine
Conditions | Yield |
---|---|
With formic acid; C24H22N4*BF4(1-)*Ru(2+)*Cl(1-)*C10H14; ammonium formate In neat (no solvent) at 40℃; for 12h; Green chemistry; chemoselective reaction; |
Cyclopropylamine
Conditions | Yield |
---|---|
Stage #1: diphenyl cyclopropylphosphoramidate With water; monoammonium para-toluenesulfonate; o-phthalic dicarboxaldehyde In acetonitrile at 90℃; for 24h; Sealed tube; Stage #2: With sodium hydroxide In water pH=8 - 9; chemoselective reaction; |
Cyclopropylamine
Conditions | Yield |
---|---|
Stage #1: N-cyclopropyl-P,P-diphenylphosphinic amide With water; monoammonium para-toluenesulfonate; o-phthalic dicarboxaldehyde In acetonitrile at 90℃; for 24h; Sealed tube; Stage #2: With sodium hydroxide In water pH=8 - 9; chemoselective reaction; |
Conditions | Yield |
---|---|
With 20 μM Tris pH 9.0 buffer at 25℃; Rate constant; |
Conditions | Yield |
---|---|
With sodium dithionite; tryptophan lyase (NosL) Y90A; S-Adenosyl-L-methionine In aq. phosphate buffer pH=7.5; Reagent/catalyst; Inert atmosphere; Enzymatic reaction; |
N-benzylcyclopropanamine
A
benzaldehyde
B
Cyclopropylamine
C
benzylamine
Conditions | Yield |
---|---|
With mitochondrial monoamine oxidase In water Mechanism; Product distribution; experiments with 14C- and 3H-labelled compounds; comparison of enzyme and electrochemical amine oxidation mechanism (two electron transfers via a radical cation intermediate); |
Conditions | Yield |
---|---|
With hydrogen azide at -72℃; Product distribution; Mechanism; Irradiation; other hydrocarbons; var. temp. and concentration of hydrogen azide; |
diethyl ether
phosphorus pentachloride
cyclopropyl methyl ketone oxime
A
methylamine
B
Cyclopropylamine
Conditions | Yield |
---|---|
Kochen des Reaktionsprodukts mit wss. KOH; |
ethyl bromoacetate
Cyclopropylamine
[(cyclopropyl)amino]acetic acid ethyl ester
Conditions | Yield |
---|---|
In ethanol for 1h; | 100% |
With triethylamine In diethyl ether at 20℃; | 100% |
In ethanol at 0 - 20℃; for 18h; | 99% |
Conditions | Yield |
---|---|
at 45℃; for 1.5h; | 100% |
at 38℃; for 2.33333h; | 91% |
In ethanol at 20℃; | 82% |
Conditions | Yield |
---|---|
With potassium carbonate In dichloromethane at 20℃; for 2.16667h; Inert atmosphere; Reflux; | 100% |
In dichloromethane at 0℃; for 2h; | 99% |
In diethyl ether at 0℃; | 97% |
propynoic acid methyl ester
Cyclopropylamine
3-(Cyclopropylamino)acrylsaeure-methylester
Conditions | Yield |
---|---|
In 1,4-dioxane at 150℃; for 0.0166667h; Flow reactor; Inert atmosphere; | 100% |
In acetonitrile 1.) 1 h, 5 - 10 deg C, 2.) 5 h, room temperature.; | 92% |
di-tert-butyl dicarbonate
Cyclopropylamine
1,1-dimethylethyl cyclopropylcarbamate
Conditions | Yield |
---|---|
In dichloromethane at 0 - 20℃; for 1h; Inert atmosphere; | 100% |
In dichloromethane at 25℃; for 2h; | 99% |
In dichloromethane at 0 - 20℃; for 18h; | 99% |
Conditions | Yield |
---|---|
In benzene for 18h; | 100% |
Stage #1: 2-Iodobenzoyl chloride; Cyclopropylamine In tetrahydrofuran for 0.166667h; Inert atmosphere; Stage #2: With triethylamine In tetrahydrofuran at 20℃; for 16h; Inert atmosphere; |
diethyl 2-ethoxymethylenemalonate
Cyclopropylamine
<(Cyclopropylamino)methylene>propanedioic acid diethyl ester
Conditions | Yield |
---|---|
In methanol at 0℃; for 0.25h; | 100% |
at 20℃; for 0.683333h; Cooling with ice; | 100% |
98.1% | |
In ethanol at 320℃; for 0.5h; | 98% |
In acetonitrile at 20 - 80℃; |
Conditions | Yield |
---|---|
for 4h; Heating; | 100% |
at 50℃; for 5h; | 84% |
With sodium carbonate In ethanol for 20h; Ambient temperature; | 59% |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 18h; | 100% |
With magnesium sulfate In dichloromethane at 20℃; for 18h; Inert atmosphere; | 100% |
at 20℃; for 2h; neat (no solvent); | 93% |
Cyclopropylamine
3-(6-chloro-9H-purin-9-yl)-1-N-[(N-tert-butyloxycarbonyl-O-carbobenzyloxy)amino]propane
3-(6-cyclopropylamino-9H-purin-9-yl)-1-N-(N-tert-butyloxycarbonylhydroxamino)propane
Conditions | Yield |
---|---|
In tetrahydrofuran for 24h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
Stage #1: cyclohexanone; Cyclopropylamine In ethanol at 20℃; for 18h; Stage #2: With hydrogen; palladium on activated charcoal at 20℃; under 2585.81 Torr; for 10h; | 100% |
With platinum(IV) oxide; hydrogen In ethanol at 20℃; under 760.051 Torr; | 66% |
With palladium on activated charcoal; hydrogen 1.) EtOH, 2.) EtOH; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
In ethanol for 6h; Heating; | 100% |
In isopropyl alcohol at 120℃; for 2h; | 90% |
In methanol | 81.4% |
In ethanol Heating; | |
In ethanol for 16h; Heating; |
Cyclopropylamine
fenoxaprop-p-ethyl
B
(R)-2-(4-hydroxyphenoxy)propionic acid ethyl ester
Conditions | Yield |
---|---|
at 20℃; | A 100% B n/a |
(1-oxiranyl-2-phenylethyl)carbamic acid tert-butyl ester
Cyclopropylamine
(1S,2R)-(1-benzyl-3-cyclopropylamino-2-hydroxypropyl)carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
In isopropyl alcohol at 50℃; for 16h; | 100% |
In isopropyl alcohol at 50℃; for 7h; | 99% |
In acetonitrile at 80℃; for 10h; | 91.4% |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane Heating; | 100% |
4-(4-isothiocyanato-phenyl)morpholine
Cyclopropylamine
N-cyclopropyl-N'-[4-(4-morpholinyl)phenyl]thiourea
Conditions | Yield |
---|---|
In ethyl acetate at 20℃; for 5.16667h; | 100% |
Cyclopropylamine
(Z)-ethyl 3-ethoxy-2-(2,3,4,5,6-pentafluorobenzoyl)acrylate
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 1.5h; | 100% |
4-(hydroxymethyl)-4-(pyrimidin-2-yl)cyclohexanone
Cyclopropylamine
(4-(cyclopropylamino)-1-(pyrimidin-2-yl)cyclohexyl)methanol
Conditions | Yield |
---|---|
Stage #1: 4-(hydroxymethyl)-4-(pyrimidin-2-yl)cyclohexanone; Cyclopropylamine With sodium tris(acetoxy)borohydride; acetic acid In acetonitrile at 0 - 25℃; for 20h; Stage #2: With sodium hydroxide; water In acetonitrile pH=~ 12; | 100% |
Conditions | Yield |
---|---|
Stage #1: C12H14N2O3; Cyclopropylamine With sodium tris(acetoxy)borohydride; acetic acid In acetonitrile at 0 - 25℃; for 3h; Stage #2: With sodium hydroxide; water In acetonitrile | 100% |
Ethyl oxalyl chloride
Cyclopropylamine
2-(cyclopropylamino)-2-oxoacetic acid ethyl ester
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 0 - 20℃; for 1h; | 100% |
Stage #1: Ethyl oxalyl chloride With pyridine In dichloromethane at 0℃; for 0.166667h; Inert atmosphere; Schlenk technique; Stage #2: Cyclopropylamine In dichloromethane at 0 - 20℃; for 2h; Inert atmosphere; Schlenk technique; | 93% |
With triethylamine In tetrahydrofuran at 0℃; for 0.166667h; | 78% |
pyridine-4-carbaldehyde
Cyclopropylamine
pyridine-4-carboxaldehyde cyclopropylimine
Conditions | Yield |
---|---|
With magnesium sulfate | 100% |
methyl 4-(2,5-dichloropyrimidin-4-yl)benzoate
Cyclopropylamine
Conditions | Yield |
---|---|
In ethanol at 80℃; | 100% |
Cyclopropylamine
Conditions | Yield |
---|---|
at 20℃; for 4h; | 100% |
3-amino-p-toluic acid
benzotriazol-1-ol
Cyclopropylamine
3-amino-N-cyclopropyl-4-methylbenzamide
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In tetrahydrofuran; DMF (N,N-dimethyl-formamide) at 54℃; for 1.83333h; | 100% |
Cyclopropylamine
4,6-dichloro-4-trifluoromethyl-1,4-dihydro-2H-3,1-benzoxazin-2-one
C11H10ClF3N2
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1h; | 100% |
3-amino-p-toluic acid
Cyclopropylamine
3-amino-N-cyclopropyl-4-methylbenzamide
Conditions | Yield |
---|---|
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap In N,N-dimethyl-formamide at 0 - 20℃; | 100% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 20℃; | 100% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In DMF (N,N-dimethyl-formamide) at 20℃; | 72% |
With dmap In water; ethyl acetate; N,N-dimethyl-formamide | 72% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 0 - 20℃; |
2-Nitrobenzenesulfonyl chloride
Cyclopropylamine
N-cyclopropyl-2-nitrobenzenesulfonamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; | 100% |
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃; for 15h; Inert atmosphere; | 93% |
With triethylamine In tetrahydrofuran at 0℃; for 1h; | 87% |
4-methoxy-3-nitro-pyridine
Cyclopropylamine
N-cyclopropyl-3-nitropyridin-4-amine
Conditions | Yield |
---|---|
at 100℃; Sealed tube; Inert atmosphere; | 100% |
With N-ethyl-N,N-diisopropylamine In ethanol for 3h; Reflux; | 72% |
With N-ethyl-N,N-diisopropylamine In ethanol for 3h; Reflux; | 72% |
5,6,7,8-Tetrahydroquinolin-8-one
Cyclopropylamine
N-cyclopropyl-5,6,7,8-tetrahydro-8-quinolinamine
Conditions | Yield |
---|---|
With sodium tris(acetoxy)borohydride; acetic acid In 1,1-dichloroethane at 20℃; for 17h; | 100% |
3-[(4-{[(tert-butoxycarbonyl)(methyl)amino]methyl}-2-phenyl-1H-pyrrol-1-yl)sulfonyl]benzoic acid
Cyclopropylamine
tert-butyl {[1-({3-[(cyclopropylamino)carbonyl]phenyl}sulfonyl)-5-phenyl-1H-pyrrol-3-yl]methyl}methylcarbamate
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 20℃; for 0.5h; | 100% |
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl-formamide at 10 - 35℃; for 0.5h; | 100% |
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