3-[[3-(dimethylamino)propyl]amino]propionitrile
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether | |
With GRACE Raney 2786 catalyst; supported palladium-based catalyst In methanol at 100℃; under 22502.3 Torr; Temperature; Pressure; |
1-amino-3-(dimethylamino)propane
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: LiAlH4 / diethyl ether View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
2,9‐bis(4-formylphenyl)‐1,10‐phenanthroline
Conditions | Yield |
---|---|
In ethanol for 5h; Reflux; | 98% |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
purpurin-18-methyl ester
Conditions | Yield |
---|---|
In toluene for 2h; Inert atmosphere; Reflux; | 97% |
2,5-dioxopyrrolidin-1-yl-3-((4R)-2-(4-methoxyphenyl)-5,5-dimethyl-1,3-dioxane-4-carboxamido)propanoate
N1-(3-dimethylaminopropyl)propane-1,3-diamine
(4R)-N-(3-(3-(3-(dimethylamino)propylamino)propylamino)-3-oxopropyl)-2-(4-methoxyphenyl)-5,5-dimethyl-1,3-dioxane-4-carboxamide
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 16h; | 85% |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
sodium dicyanamide
Cu(N,N-dimethyldipropyltriamine)(dicyanamide)2
Conditions | Yield |
---|---|
In water aq. soln. of sodium dicyanoamide added to preheated aq. soln. of Cu(NO3)2*3H2O and amine, heated on steam-bath for 15 min; filtered through Celite, filtrate stored at room temp. for 1 wk, ppt. filtered off, washed with 2-propanol and ether, air dried; elem. anal.; | 78% |
sodium tetrafluoroborate
fac-[ReI(OH2)3(CO)3](SO3CF3)
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
In water aq. soln. of Re complex was treated with ligand; pH was adjusted to 6; MeOH was added to dissolve ppt.; refluxed for 16 h; cooled to room temp.;solid Na salt was added; kept for 2-3 d; | 56% |
4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3-buten-2-one
N1-(3-dimethylaminopropyl)propane-1,3-diamine
N-<3-Dimethylamino-propyl>-N'-<1-methyl-3-(2,6,6-trimethyl-cyclohexen-(1)-yl)-propyl>-1,3-propandiamin
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol at 100℃; under 51.7 Torr; |
(2E,4E)-4-Methyl-6-(2,6,6-trimethyl-cyclohex-1-enyl)-hexa-2,4-dienal
N1-(3-dimethylaminopropyl)propane-1,3-diamine
N-<3-Dimethylamino-propyl>-N'-<4-methyl-6-(2,6,6-trimethyl-cyclohexen-(1)-yl)-hexyl>-1,3-propandiamin
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol at 100℃; under 51.7 Torr; |
alpha-ionone
N1-(3-dimethylaminopropyl)propane-1,3-diamine
N-<3-Dimethylamino-propyl>-N'-<1-methyl-3-(2,6,6-trimethyl-cyclohexen-(2)-yl)-propyl>-1,3-propandiamin
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol at 100℃; under 51.7 Torr; |
2-methyl-4-(2,6,6-trimethylcyclohex-1-en-1-yl)-2-butenal
N1-(3-dimethylaminopropyl)propane-1,3-diamine
N-<3-Dimethylamino-propyl>-N'-<2-methyl-4-(2,6,6-trimethyl-cyclohexen-(1)-yl)-butyl>-1,3-propandiamin
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol at 100℃; under 51.7 Torr; |
3-isopropenyl-1-methyl-2-(3-oxobutyl)-cyclopent-1-ene
N1-(3-dimethylaminopropyl)propane-1,3-diamine
N-<3-Dimethylamino-propyl>-N'-<1-methyl-3-(5-isopropyl-2-methyl-cyclopenten-(1)-yl)-propyl>-1,3-propandiamin
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol at 100℃; under 51.7 Torr; |
2,6-Dimethyl-8-<1,3,3-trimethyl-cyclohexen-(1)-yl-(2)>-octatrien-(2,4,6)-al
N1-(3-dimethylaminopropyl)propane-1,3-diamine
N-<3-Dimethylamino-propyl>-N'-<2,6-dimethyl-8-(2,6,6-trimethyl-cyclohexen-(1)-yl)-octyl>-1,3-propandiamin
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol at 100℃; under 51.7 Torr; |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
tetrahydroionone
Conditions | Yield |
---|---|
With hydrogen; nickel In ethanol at 100℃; under 51.7 Torr; |
endo-N-hydroxy-5-norbornene-2,3-dicarboximide O-bromoacetate
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
In water; acetone at 20℃; for 0.266667h; Sonication; |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: acetone; H2O / 0.27 h / 20 °C / Sonication 2: aq. triethylammonium bicarbonate buffer / acetone / 1 h / 20 °C / pH 8.5 View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
N'-{3-[(3-aminopropyl)amino]propyl}-N,N-dimethylpropane-1,3-diamine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: LiAlH4 / diethyl ether View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 2: LiAlH4 / diethyl ether 3: (i) , (ii) LiAlH4, Et2O View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
In water; acetone pH=10; |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride
N,N'-bis[7-(dimethylamino)-4-azaheptyl]-3,4,9,10-perylenetetracarboxylic diimide
Conditions | Yield |
---|---|
In 1,4-dioxane; N,N-dimethyl acetamide for 6h; Heating; |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
1,4,7-tris(tert-butoxycarbonylmethyl)-1,4,7,10-tetraazacyclododecane-10-acetic acid
C36H71N7O7
Conditions | Yield |
---|---|
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 1.5h; | |
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 1.5h; |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
2-{[1-{4-[3-(DOTA-amino-propyl)-(3-dimethylamino-propyl)-carbamoyl]-2-isopropyl-phenyl}-5-(2,6-dimethoxy-phenyl)-1H-pyrazole-3-carbonyl]-amino}-adamantane-2-carboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 1.5 h 2.1: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.75 h 3.1: water; lithium hydroxide / 1,4-dioxane / 5 h 3.2: pH 4 4.1: HATU; N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 0.08 h 4.2: 25 h / 20 - 65 °C 5.1: triisobutylsilane / dichloromethane / 3.5 h / 20 °C 6.1: aq. acetate buffer / 0.5 h / 90 °C View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
1-{4-[(3-DOTA(tBu)3-aminopropyl)-(3-dimethylaminopropyl)carbamoyl]-2-isopropylphenyl}-5-(2,6-dimethoxyphenyl)-1H-pyrazole-3-carboxylic acid methyl ester
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 1.5 h 2: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.75 h View Scheme | |
Multi-step reaction with 2 steps 1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1.5 h 2: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.75 h View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
1-{4-[(3-DOTA(tBu)3-aminopropyl)-(3-dimethylaminopropyl)carbamoyl]-2-isopropylphenyl}-5-(2,6-dimethoxyphenyl)-1H-pyrazole-3-carboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 1.5 h 2.1: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.75 h 3.1: water; lithium hydroxide / 1,4-dioxane / 5 h 3.2: pH 4 View Scheme | |
Multi-step reaction with 3 steps 1.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1.5 h 2.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.75 h 3.1: water; lithium hydroxide / 1,4-dioxane / 5 h 3.2: pH 4 View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
2-{[1-{4-[(3-DOTA(tBu)3-aminopropyl)-(3-dimethylaminopropyl)carbamoyl]-2-isopropylphenyl}-5(2,6-dimethoxyphenyl)-1H-pyrazole-3-carbonyl]amino}adamantane-2-carboxylic acid
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 1.5 h 2.1: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.75 h 3.1: water; lithium hydroxide / 1,4-dioxane / 5 h 3.2: pH 4 4.1: HATU; N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 0.08 h 4.2: 25 h / 20 - 65 °C View Scheme | |
Multi-step reaction with 4 steps 1.1: benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 1.5 h 2.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 0.75 h 3.1: water; lithium hydroxide / 1,4-dioxane / 5 h 3.2: pH 4 4.1: N-ethyl-N,N-diisopropylamine; HATU / 1-methyl-pyrrolidin-2-one / 24 h / 20 - 65 °C View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 1.5 h 2.1: HATU; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.75 h 3.1: water; lithium hydroxide / 1,4-dioxane / 5 h 3.2: pH 4 4.1: HATU; N-ethyl-N,N-diisopropylamine / 1-methyl-pyrrolidin-2-one / 0.08 h 4.2: 25 h / 20 - 65 °C 5.1: triisobutylsilane / dichloromethane / 3.5 h / 20 °C View Scheme |
N1-(3-dimethylaminopropyl)propane-1,3-diamine
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In dichloromethane |
N'-(3-AMINOPROPYL)-N,N-DIMETHYL-PROPANE-1,3-DIAMINE's Molecular formula: C8H21N3
N'-(3-AMINOPROPYL)-N,N-DIMETHYL-PROPANE-1,3-DIAMINE's Molar mass: 159.27
EINECS: 234-148-4
Flash point: 220 °F
Boiling point: 220 °C(lit.)
density 0.883 g/mL at 25 °C(lit.)
refractive index: n20/D 1.4630(lit.)
Synonyms: 3-Propanediamine, N'-(3-aminopropyl)-N,N-dimethyl-1; N,N-Dimethyldipropyltriamine; 3-Propanediamine,N'-(3-aminopropyl)-N,N-dimethyl-1; n'-(3-aminopropyl)-n,n-dimethyl-1,3-propanediamine; n'-(3-aminopropyl)-n,n-dimethyl-3-propanediamine; N N'-N,N-Dimethyldipropylenetriamine (ATOFI&; 3-(3-Dimethylaminopropylamino)propylamine; N-(3-Dimethylaminopropyl)propane-1,3-diamine; N,N-N,N-Dimethyldipropylenetriamine (ATOFINA DMAPAPA), 99%
1. | orl-unr LD50:1432 mg/kg | GTPZAB Gigiena Truda i Professionalnye Zabolevaniia. Labor Hygiene and Occupational Diseases. 28 (11)(1984),50. | ||
2. | ipr-unr LD50:72 mg/kg | GTPZAB Gigiena Truda i Professionalnye Zabolevaniia. Labor Hygiene and Occupational Diseases. 28 (11)(1984),50. |
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