Conditions | Yield |
---|---|
With titanium(III) chloride In water for 1h; Ambient temperature; | 76% |
With ethanol; sodium | |
With zinc In acetic acid |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether at 0 - 10℃; for 3h; 1) R.T., 1 h 2) reflux, 3 h; | A 31% B 1.0 g |
With lithium aluminium tetrahydride In diethyl ether at 0 - 10℃; for 3h; 1) R.T., 1 h 2) reflux, 3 h; | A 31% B 31% |
Conditions | Yield |
---|---|
With chloroamine | |
With potassium hydroxide; hydroxylamine-O-sulfonic acid In water for 0.166667h; Heating; | |
With ammonium acetate; hydrogenchloride; sodium nitrite In methanol; water |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With ethanol; hydrazine hydrate |
Conditions | Yield |
---|---|
With titanium(III) chloride; ammonium acetate In water for 1h; Product distribution; Ambient temperature; variation of reaction conditions ( pH<1, pH=9.4 ); | A 3 % Chromat. B 86 % Chromat. |
With hydrogenchloride; zinc In water for 24h; Product distribution; Ambient temperature; | A 8 % Chromat. B 98 % Chromat. |
With potassium hydroxide; aluminium In water for 24h; Product distribution; Ambient temperature; | A 43 % Chromat. B 64 % Chromat. |
Conditions | Yield |
---|---|
With acetic acid In acetonitrile Product distribution; Mechanism; |
Conditions | Yield |
---|---|
With acetic acid; zinc |
ethanol
hydrazine hydrate
3-oxa-1,5-dichloropentane
1-aminomorpholine
water
hydrazine hydrate
3-oxa-1,5-dichloropentane
A
1-aminomorpholine
B
4,4'-bimorpholine
A
1-aminomorpholine
Conditions | Yield |
---|---|
With H2O or aq. mineral acid decompn. with H2O or dild. aq. mineral acid; | |
decompn. on heating; | |
decompn. on heating; | |
With H2O or aq. mineral acid decompn. with H2O or dild. aq. mineral acid; |
O(CH2CH2)2NNH2*BH3
water
A
1-aminomorpholine
B
hydrogen
C
boric acid
Conditions | Yield |
---|---|
In water | |
In water |
1-aminomorpholine
p-toluenesulfonyl chloride
4-methyl-N-morpholin-4-ylbenzenesulfonamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 4℃; | 100% |
In tetrahydrofuran at 20℃; for 3h; Inert atmosphere; | 17 mg |
1-aminomorpholine
1-(2,4-dichlorophenyl)-6-methyl-1H-benzofuro[3,2-0c]pyrazole-3-carboxylic acid
N-(morpholin-1-yl)-1-(2,4-dichlorophenyl)-6-methyl-1H-benzofuro[3,2-c]pyrazole-3-carbohydrazide
Conditions | Yield |
---|---|
Stage #1: 1-(2,4-dichlorophenyl)-6-methyl-1H-benzofuro[3,2-0c]pyrazole-3-carboxylic acid With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In dichloromethane at 20℃; for 1h; Stage #2: 1-aminomorpholine In dichloromethane at 20℃; for 22h; | 100% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 120℃; for 0.1h; Temperature; Reagent/catalyst; Solvent; Mannich Aminomethylation; Microwave irradiation; | 100% |
1-aminomorpholine
5-ethylfurfural
[1-(5-Ethyl-furan-2-yl)-meth-(E)-ylidene]-morpholin-4-yl-amine
Conditions | Yield |
---|---|
In ethanol for 0.5h; heating on a steam bath; | 99% |
1-aminomorpholine
4-methoxyphenylboronic acid
4-methoxy-N-morpholinobenzenesulfonamide
Conditions | Yield |
---|---|
With DABCO-bis(sulfur dioxide); tetrabutylammomium bromide; oxygen; palladium diacetate In 1,4-dioxane at 80℃; for 12h; | 99% |
1-aminomorpholine
diethoxydiphenylsilane
N‐morpholinobenzenesulfonamide
Conditions | Yield |
---|---|
With 1,4-diazabicyclo[2.2.2]octane-triethylenediamine-bis(sulfur dioxide); oxygen; copper diacetate; cesium fluoride; XPhos In 1,4-dioxane at 80℃; | 99% |
1-aminomorpholine
Conditions | Yield |
---|---|
With 1,4-diazabicyclo[2.2.2]octane-triethylenediamine-bis(sulfur dioxide) In acetonitrile at 25℃; for 0.166667h; Inert atmosphere; | 99% |
1-aminomorpholine
Methyl 3-formylbenzoate
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 22h; Inert atmosphere; | 99% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 24h; Inert atmosphere; | 99% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; | 94% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 18h; Inert atmosphere; | 99% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; | 92% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; | 92% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With hydrogenchloride for 0.116667h; Time; Microwave irradiation; | 99% |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 16h; Inert atmosphere; | 99% |
1-aminomorpholine
diethyl 2-ethoxymethylenemalonate
(morpholinyl-4 amino)-3 ethoxycarbonyl-2 propenoate d'ethyle
Conditions | Yield |
---|---|
In methanol for 1h; Ambient temperature; | 98% |
1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-5-methyl-1H-imidazole-4-carboxylic acid
1-aminomorpholine
Conditions | Yield |
---|---|
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In acetonitrile at 20℃; for 16h; | 98% |
1-aminomorpholine
2-Methylphenylboronic acid
2-methyl-N-morpholinobenzenesulfonamide
Conditions | Yield |
---|---|
With DABCO-bis(sulfur dioxide); tetrabutylammomium bromide; oxygen; palladium diacetate In 1,4-dioxane at 80℃; for 12h; | 98% |
Conditions | Yield |
---|---|
With DABCO-bis(sulfur dioxide); tetrabutylammomium bromide; oxygen; palladium diacetate In 1,4-dioxane at 80℃; for 12h; | 98% |
1-aminomorpholine
3,3-diethyl-1-(4-methylphenyl)-1-triazene
4-methyl-N-morpholin-4-ylbenzenesulfonamide
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; sulfur dioxide In acetonitrile at 60℃; for 3h; Inert atmosphere; Schlenk technique; | 98% |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; | 98% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; | 93% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane at 20℃; for 20h; Inert atmosphere; | 98% |
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; | 83% |
With magnesium sulfate In dichloromethane at 20℃; |
Conditions | Yield |
---|---|
Stage #1: 1-aminomorpholine; carbon disulfide; 3-chloroprop-1-ene With potassium carbonate In neat liquid at 0 - 20℃; Green chemistry; Stage #2: With iodine In neat liquid at 20℃; for 0.3h; Green chemistry; | 98% |
IUPAC Name: Morpholin-4-amine
Molecular Formula: C4H10N2O
Molecular Weight: 102.14 g/mol
Canonical SMILES: N1(CCOCC1)N
InChI: InChI=1/C4H10N2O/c5-6-1-3-7-4-2-6/h1-5H2
Mol File: 4319-49-7.mol
EINECS: 224-347-4
Classification Code: Mutation data
Product Categories: Variousamine; Aromatic Morpholines; Amines;Morpholines & Thiomorpholines; Morpholines & Thiomorpholines; Building Blocks; Heterocyclic Building Blocks; Morpholines
Water Solubility: miscible
logP(octanol-water): -1.580
XLogP3: -1.1
H-Bond Donor: 1
H-Bond Acceptor: 3
Rotatable Bond Count: 0
Exact Mass: 102.079313
MonoIsotopic Mass: 102.079313
Topological Polar Surface Area: 38.5
Heavy Atom Count: 7
Complexity: 51.7
Index of Refraction: 1.477
Molar Refractivity: 27.17 cm3
Molar Volume: 96.1 cm3
Polarizability: 10.77×10-24cm3
Surface Tension: 36.9 dyne/cm
Density: 1.062 g/cm3
Flash Point: 58.3 °C
Enthalpy of Vaporization: 40.44 kJ/mol
Boiling Point: 168 °C at 760 mmHg
Atmospheric OH Rate Constant: 7.48E-11 cm3/molecule-sec at 25 °C
Vapour Pressure of 4-Morpholinamine (CAS NO.4319-49-7): 1.65 mmHg at 25 °C
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | oral | > 1gm/kg (1000mg/kg) | Farmaco. Vol. 45, Pg. 223, 1990. |
Hazard Codes: Xn.F.Xi
Risk Statements: 20/21/22-36/37/38
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38: Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36-23-16
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36: Wear suitable protective clothing.
S23: Do not breathe vapour.
S16: Keep away from sources of ignition.
RIDADR: UN 1993 3/PG 3
WGK Germany: 3
Hazard Note: Harmful
HazardClass: 3
PackingGroup of 4-Morpholinamine (CAS NO.4319-49-7): III
4-Morpholinamine (CAS NO.4319-49-7), its Synonyms are Morpholin-4-ylamine ; Morpholine, 4-amino- ; 4-27-00-00623 (Beilstein Handbook Reference) ; 4-Aminomorpholine ; Morpholine, 4-amino- ; N-Aminomorpholine . It is clear colorless to faintly yellow liquid.
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