Conditions | Yield |
---|---|
at 55℃; under 225.023 - 31503.2 Torr; for 0.666667h; Pressure; Autoclave; Green chemistry; | 98.99% |
In water at 30℃; for 4 - 5h; | 92.7% |
unter Kuehlung; |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With sulfuric acid; water at 100℃; for 8h; Hydrolysis; | 95% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 17 - 42℃; for 0.270167h; | 82.4% |
With sodium hydrogencarbonate; sodium hydroxide In water at 50 - 65℃; under 1125.11 Torr; for 4.33333h; Product distribution / selectivity; |
oxiranyl-methanol
methylamine
A
3-methylamino-propane-1,2-diol
B
2-(methylamino)-1,3-propanediol
3-(N-Benzyl-N-methylamino)-1,2-propanediol
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With hydrogen | |
With hydrogen; palladium on activated charcoal In methanol under 2585.7 Torr; for 18h; |
N,N'-bis(2,3-dihydroxypropyl)-5-{2-[(2,3-dihydroxypropyl)methylamino]-2-oxoethoxy}-1,3-benzenedicarboxamide
A
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With water at 95℃; Rate constant; |
oxiranyl-methanol
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
In water; methylamine | |
With methylamine In water | 25.6g (76%) |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With carbon dioxide; water at 140℃; under 22502.3 Torr; for 12h; Autoclave; |
3-methylamino-propane-1,2-diol
(2′Z-3′E)-6-bromoindirubin-3′-[O-(2-bromoethyl)oxime]
(2'Z-3'E)-6-bromoindirubin-3'-(O-{2-[N-methyl,N-(2,3-dihydroxypropyl)amino]ethyl}oxime)
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 50℃; | 100% |
In N,N-dimethyl-formamide at 90℃; for 0.666667h; Inert atmosphere; Microwave irradiation; |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With nitrogen(II) oxide; sodium methylate In methanol; diethyl ether at 20℃; under 4654.46 Torr; | 98.9% |
With nitrogen(II) oxide; sodium methylate In methanol; diethyl ether |
5-Acetoxyacetylamino-2,4,6-tribromo-3-[N-(2,3-diacetoxypropyl)carbamoyl] benzoyl chloride
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
In acetone | 98% |
3-methylamino-propane-1,2-diol
5-methoxyacetylamino-2,4,6-triiodoisophthalic acid (2,3-diacetoxypropyl)amide chloride
5-methoxyacetylamino-2,4,6-triiodoisophthalic acid [(2,3-dihydroxy-N-methylpropyl)-(2,3-diacetoxypropyl)]diamide
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl acetamide Product distribution / selectivity; | 98% |
With triethylamine In ISOPROPYLAMIDE at 20℃; for 2h; |
ethyl 1-imidazolecarboxylate
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With potassium carbonate In tetrahydrofuran for 15h; Reflux; | 98% |
3-methylamino-propane-1,2-diol
trifluoroacetic acid
Conditions | Yield |
---|---|
Stage #1: 3-methylamino-propane-1,2-diol; (R)-1-(3-((3'-(3-bromopropoxy)-2,2'-dimethyl-[1,1'-biphenyl]-3-yl)oxy)propyl)pyrrolidin-3-ol With N-ethyl-N,N-diisopropylamine In methanol at 65℃; Inert atmosphere; Stage #2: trifluoroacetic acid In water; acetonitrile | 98% |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; methanol at 65℃; for 72h; Inert atmosphere; | 98% |
5-Amino-3-acetoxymethyl-2,4,6-triiodobenzoyl chloride
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
97% | |
97% |
5-acetoxyacetylamino-2,4,6-tribromo-3-carbamoylbenzoyl chloride
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
In acetone | 97% |
Conditions | Yield |
---|---|
With sulfuric acid; water at 100℃; for 8h; Hydrolysis; | 95% |
3-methylamino-propane-1,2-diol
2,4,6-Tribromo-5-bromomethanesulfonylamino-N-(2,3-dihydroxypropyl)-N-methyl-N'-(2,3-diacetoxypropyl)-isophthalamide
Conditions | Yield |
---|---|
In acetone | 95% |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In 1,2-dimethoxyethane for 18h; Reflux; Large scale; | 95% |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine Large scale; | 95% |
3-methylamino-propane-1,2-diol
C18H27N3O8
Conditions | Yield |
---|---|
With sodium t-butanolate In methanol for 48h; Reagent/catalyst; Reflux; | 92.3% |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
In 1,4-dioxane; acetonitrile at 20℃; | 91% |
In 1,4-dioxane; acetonitrile at 20℃; | 60 g |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
Stage #1: 3-nitro-5-(((2-oxo-1,3-dioxolan-4-yl)methyl)carbamoyl)benzoic acid With oxalyl dichloride In dichloromethane at 0 - 20℃; for 1h; Stage #2: 3-methylamino-propane-1,2-diol In ethanol; dichloromethane at -10℃; for 2.5h; | 90% |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl acetamide at 20℃; for 10h; | 90% |
With triethylamine In N,N-dimethyl acetamide at 20℃; for 10h; | 90% |
5-nitro-1,3-benzenedicarboxylic acid, monomethyl ester
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With potassium tert-butylate In tert-butyl alcohol Inert atmosphere; Reflux; | 89% |
In acetonitrile at 75 - 80℃; for 5h; | 80% |
Conditions | Yield |
---|---|
In dichloromethane for 0.5h; | 88.9% |
2-chloro-6-methoxy-3-nitropyridine
3-methylamino-propane-1,2-diol
3-[(6-methoxy-3-nitro-pyridin-2-yl)methyl-amino]propane-1,2-diol
Conditions | Yield |
---|---|
In ethanol for 2h; Heating / reflux; | 87.1% |
3-methylamino-propane-1,2-diol
[(3-acetoxy-1-acetylindol-2-yl)methylene]malononitrile
1-acetyl-2-[2-cyano-2-(5-hydroxymethyl-3-methyloxazolidin-2-ylidene)ethylidene]indolin-3-one
Conditions | Yield |
---|---|
In isopropyl alcohol for 1h; Reflux; | 86.7% |
5-Methoxyacetamido-2,4,6-triiodoisophthaloyl chloride
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With ZrO2-Cr2O3 solid base catalyst In N,N-dimethyl acetamide at 10 - 15℃; for 5h; | 85% |
3-methylamino-propane-1,2-diol
α-isocyanato-L-O-methyltyrosine methyl ester
(2RS)-<<(2,3-dihydroxypropyl)methylamino>carbonyl>-O-methyltyrosine methyl ester
Conditions | Yield |
---|---|
In 1,4-dioxane 1.) 0 deg C, 1 h, 2.) RT, 1 h; | 84% |
Conditions | Yield |
---|---|
With potassium hydroxide In toluene Heating; | 82% |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 100℃; for 16h; | 82% |
3-methylamino-propane-1,2-diol
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 0.166667h; | 81% |
4-methyleneoxetan-2-one
3-methylamino-propane-1,2-diol
N-(2,3-dihydroxypropyl)-3-oxobutanamide
Conditions | Yield |
---|---|
In tetrahydrofuran at -5 - 0℃; for 1h; | 79% |
3-methylamino-propane-1,2-diol
4-[(3-bromophenyl)-amino]-6-fluoropyrido[3,4-d]pyrimidine
Conditions | Yield |
---|---|
In dimethyl sulfoxide at 80℃; for 24h; | 72% |
3-Methylamino-1,2-Propanediol(40137-22-2) is also named as N-METHYL-3-AMINO-1,2-PROPANEDIOL;3-(AMINOMETHYL)-1,2-PROPANEDIOL;2,3-Dihydroxy-N-methylpropylamine;3-Methylamino-1,2-Propandiol;N-Methyl-2,3-dihydroxypropylamine;1,2-Propanediol, 3-(methylamino)-;ZINC04283843;CID7167892,and so on.3-Methylamino-1,2-Propanediol(40137-22-2) at room temperature is usually a colorless to light yellow liquid.
CAS: 40137-22-2
Molecular Formula: C4H11NO2
Molecular Weight: 105.14
Molecular structure:
EINECS: 254-809-0
Water Solubility: miscible
BRN: 1733341
ACD/LogD (pH 5.5): -4.63
ACD/LogD (pH 7.4): -3.6
ACD/BCF (pH 5.5): 1
ACD/BCF (pH 7.4): 1
ACD/KOC (pH 5.5): 1
ACD/KOC (pH 7.4): 1
H bond acceptors: 3
H bond donors: 3
Freely Rotating Bonds: 5
Index of Refraction: 1.463
Molar Refractivity: 27.2 cm3
Molar Volume: 98.7 cm3
Polarizability: 10.78 10-24cm3
Surface Tension: 41.1 dyne/cm
Density: 1.064 g/cm3
Flash Point: 142.7 °C
Enthalpy of Vaporization: 56.11 kJ/mol
Boiling Point: 245.8 °C at 760 mmHg
Vapour Pressure: 0.00467 mmHg at 25°C
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