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:4461-39-6
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inquiryProduct Name: n-(2-hydroxyethyl)-1,N,N'-Bis(3-aminopropyl)ethylenediamine Molecular Formula: C5H14N2O Molecular Weight: 118.17 CAS RN: 4461-39-6 Properties: colorless transparent liquid,b.p.: 255℃ Use: As intermediate for organic synthesis
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inquiryN-(2-Hydroxyethyl)-1,3-propanediamine CAS: 4461-39-6 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 qua
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inquiryProduct Detail Minimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,
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inquirylow price high quality high purity good sevice stock Appearance:white Storage:Preserve In Well-Closed, Light-Resistant and Tight Containers. Store In Cool & Dry Place Package:1g,5g,10g...1kg,5kg...more Application:Pharmaceutical interme
Cas:4461-39-6
Min.Order:1 Gram
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inquiryPacking: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once Transportation:Express/Sea/Air Port:Ningbo/Shanghai/Qingd
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inquiryProduct Name: N-(2-Hydroxyethyl)-1,3-propanediamine Synonyms: N-(2-HYDROXYETHYL)-1,3-DIAMINOPROPANE;N-(2-HYDROXYETHYL)-1,3-PROPANEDIAMINE;N-(2-HYDROX…Appearance:Solid powder Storage:Sealed,light and oxygen resistant Package:aluminum foil bag,carton
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inquiry3-<(2-hydroxyethyl)amino>propionitrile
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
With rhodium(III) oxide; gold oxide; hydrogen at 82 - 83℃; under 15001.5 Torr; for 18h; Pressure; | 98.2% |
With ethanol; ammonia; nickel at 120℃; under 66195.7 Torr; Hydrogenation; |
oxirane
Trimethylenediamine
A
2-[(3-aminopropyl)amino]ethanol
B
N,N'-bis(2-hydroxyethyl)-1,3-propanediamine
Conditions | Yield |
---|---|
In methanol at 0℃; | A 60% B 20% |
Conditions | Yield |
---|---|
With perchloric acid at 25℃; Rate constant; Thermodynamic data; E(a), ΔS(excit.); |
2-[(3-aminopropyl)amino]ethanol
9,10-Dihydroxy-2,3-dihydro-anthracene-1,4-dione
1,4-bis({3-[(2-hydroxyethyl)amino]-propyl}amino)-9,10-dihydroanthracene-9,10-dione
Conditions | Yield |
---|---|
Stage #1: 2-[(3-aminopropyl)amino]ethanol; 9,10-Dihydroxy-2,3-dihydro-anthracene-1,4-dione In acetonitrile at 50℃; for 1h; Inert atmosphere; Stage #2: With air at 50℃; for 1h; | 99% |
2-[(3-aminopropyl)amino]ethanol
dibromohydrate du N-(bromoethyl-2)diamino-1,3 propane
Conditions | Yield |
---|---|
Stage #1: 2-[(3-aminopropyl)amino]ethanol With hydrogen bromide In sulfolane at 90 - 119℃; Stage #2: With phosphorus tribromide In sulfolane at 120℃; for 1h; Product distribution / selectivity; | 96% |
2-[(3-aminopropyl)amino]ethanol
2-(3-aminopropylamino)ethyl bromide
Conditions | Yield |
---|---|
Stage #1: 2-[(3-aminopropyl)amino]ethanol With hydrogen bromide In ethanol at 13 - 15℃; for 2h; Stage #2: In methanol for 1h; Time; Reflux; | 91% |
Conditions | Yield |
---|---|
With phosphorus pentachloride In tetrachloromethane at 30 - 60℃; for 20h; Inert atmosphere; | 90% |
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
at 20℃; for 96h; | 85% |
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In chloroform for 22h; Reflux; Inert atmosphere; | 84% |
7-chloro-3-(3,4-dichlorophenyl)-3,4-dihydro-10-hydroxy-1,9(2H,10H)-acridinedione
2-[(3-aminopropyl)amino]ethanol
7-Chloro-3-(3,4-dichloro-phenyl)-10-hydroxy-1-[(E)-3-(2-hydroxy-ethylamino)-propylimino]-1,3,4,10-tetrahydro-2H-acridin-9-one
Conditions | Yield |
---|---|
In ethanol for 1.5h; Heating; | 83% |
carbon disulfide
2-[(3-aminopropyl)amino]ethanol
3-Benzyloxybenzaldehyde
copper(II) acetate monohydrate
Conditions | Yield |
---|---|
Stage #1: 2-[(3-aminopropyl)amino]ethanol; 3-Benzyloxybenzaldehyde With carbon disulfide In methanol at 20℃; for 2h; Stage #2: carbon disulfide In methanol for 0.666667h; Stage #3: copper(II) acetate monohydrate In methanol for 4h; | 81% |
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In chloroform for 3.5h; Reflux; Inert atmosphere; | 76% |
2-[(3-aminopropyl)amino]ethanol
di-tert-butyl dicarbonate
(3-tert-BOCamino-propyl)-(2-hydroxy-ethyl)-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 71% |
4-chloro-2-(4-methoxyphenyl)-pyrimido[5,4-c]cinnoline
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In ethanol for 0.333333h; Heating; | 68% |
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
Stage #1: 2-[(3-aminopropyl)amino]ethanol; 2-(3-cyanobenzyloxy)-4-(2-methyl-(1,1’-diphenyl)-3-yl-methoxyl)benzaldehyde With iodine; potassium carbonate In tert-butyl alcohol at 70℃; for 3h; Stage #2: With hydrogenchloride In water; acetonitrile for 0.333333h; | 67% |
Conditions | Yield |
---|---|
In water for 12h; Ambient temperature; | 66% |
2-[(3-aminopropyl)amino]ethanol
benzyl chloroformate
{3-[Benzyloxycarbonyl-(2-hydroxy-ethyl)-amino]-propyl}-carbamic acid benzyl ester
Conditions | Yield |
---|---|
With sodium hydroxide at 0 - 20℃; for 25h; | 64% |
2-[(3-aminopropyl)amino]ethanol
AF 1311TS
Conditions | Yield |
---|---|
Stage #1: AF 1311TS With 1,1'-carbonyldiimidazole In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: 2-[(3-aminopropyl)amino]ethanol In N,N-dimethyl-formamide at 20℃; for 24h; | 64% |
5-(biphenyl-4-yl)-1,3,4-oxadiazole-2-carboxylic acid ethyl ester
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 63% |
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In methanol; water pH 8; | 60% |
2-[(3-aminopropyl)amino]ethanol
2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile
(3-tert-BOCamino-propyl)-(2-hydroxy-ethyl)-carbamic acid tert-butyl ester
Conditions | Yield |
---|---|
In tetrahydrofuran for 12h; Ambient temperature; | 58% |
2-[(3-aminopropyl)amino]ethanol
1-(3-chlorophenylmethyl)-1H-indazole-3-carboxylic acid
Conditions | Yield |
---|---|
Stage #1: 1-(3-chlorophenylmethyl)-1H-indazole-3-carboxylic acid With 1,1'-carbonyldiimidazole In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: 2-[(3-aminopropyl)amino]ethanol In N,N-dimethyl-formamide at 20℃; for 24h; | 58% |
4-chloro-2-phenyl-pyrimido[5,4-c]cinnoline
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In ethanol for 0.333333h; Heating; | 57% |
3-(biphenyl-4-yl)-1,2,4-oxadiazole-5-carboxylic acid ethyl ester
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 56% |
3-(4-trifluoromethylphenyl)-7-chloro-10-hydroxy-3,4-dihydroacridine-1,9(2H,10H)-dione
2-[(3-aminopropyl)amino]ethanol
7-Chloro-10-hydroxy-1-[(E)-3-(2-hydroxy-ethylamino)-propylimino]-3-(4-trifluoromethyl-phenyl)-1,3,4,10-tetrahydro-2H-acridin-9-one
Conditions | Yield |
---|---|
In benzene for 2h; Heating; | 53% |
2-[(3-aminopropyl)amino]ethanol
(1S,3'S,5'S)-N-(2-cyclohexyl-1-(3-isopropyl-2-oxo-2,3,4,5-tetrahydrofuran-5-yl)ethyl)-(1S)-(1-((4-(methoxymethoxy)piperidin-1-yl)carbonyl)-2-phenylethyl)-L-norleucinamide
Conditions | Yield |
---|---|
With acetic acid at 85℃; for 24h; | 52% |
2-[(3-aminopropyl)amino]ethanol
1-(2-chlorophenylmethyl)-1H-indazole-3-carboxylic acid
Conditions | Yield |
---|---|
Stage #1: 1-(2-chlorophenylmethyl)-1H-indazole-3-carboxylic acid With 1,1'-carbonyldiimidazole In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: 2-[(3-aminopropyl)amino]ethanol In N,N-dimethyl-formamide at 20℃; for 24h; | 44% |
Glyoxal
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In water Ambient temperature; | A 11% B 38% |
4-chloro-2-(2-furyl)-pyrimido[5,4-c]cinnoline
2-[(3-aminopropyl)amino]ethanol
Conditions | Yield |
---|---|
In ethanol for 0.333333h; Heating; | 36% |
2-[(3-aminopropyl)amino]ethanol
N-(1-Methyl-5-nitro-1H-imidazol-2-yl)-formimidic acid ethyl ester
C15H22N10O5
Conditions | Yield |
---|---|
In benzene Heating; | 30% |
2-[(3-aminopropyl)amino]ethanol
urea
1-(2-hydroxyethyl)tetrahydropyrimidin-2(1H)-one
Conditions | Yield |
---|---|
In neat (no solvent) at 130℃; for 10h; Sealed tube; | 14% |
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