(R)-3-Methylmorpholine supplier

Name
(R)-3-Methylmorpholine
EINECS
CAS No. 74572-04-6
Article Data10
CAS DataBase
Density 0.891 g/cm³
Solubility
Melting Point
Formula C₅H₁₁NO
Boiling Point 137.1 °C at 760 mmHg
Molecular Weight 101.148
Flash Point 41.3 °C
Transport Information
Appearance
Safety
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms Morpholine,3-methyl-, (R)-;(3R)-3-Methylmorpholine;(R)-3-Methylmorpholine;
PSA 21.26000
LogP 0.32350

Synthetic route

: 954133-47-2
(R)-4-(4-methoxybenzyl)-3-methylmorpholine

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
With palladium on activated charcoal; hydrogen In methanol at 50℃; under 9500.64 Torr; for 18h;	83%

: 119844-67-6
(5R)-5-methylmorpholin-3-one

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 16h;	75%
Stage #1: (5R)-5-methylmorpholin-3-one With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; for 15.5h; Heating / reflux; Stage #2: With hydrogenchloride; ethanol In tetrahydrofuran

: (R)-2-(2-hydroxyethylamino)propan-1-ol

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
Stage #1: (R)-2-(2-hydroxyethylamino)propan-1-ol With sulfuric acid at 140℃; for 14h; Stage #2: With sodium hydroxide In water at 0℃;	65%

: 122116-12-5
2-(prop-2-yn-1-yloxy)ethan-1-amine

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
Stage #1: 2-(prop-2-yn-1-yloxy)ethan-1-amine With C42H58N4O2Ti In toluene at 110℃; for 14h; Inert atmosphere; Schlenk technique; Stage #2: With formic acid; [{(1S,2S-N-p-toluenesulfonyl-1,2-diphenylethanediamine)}(η6-p-cymene)RuCl]; triethylamine In N,N-dimethyl-formamide; toluene at 20℃; for 14h; Inert atmosphere; Schlenk technique; enantioselective reaction;	65%
Multi-step reaction with 2 steps 1: bis(N-2,6-diisoprpylphenylbenzamidato)bis(dimethylamido)titanium (IV) / toluene / 14 h / 110 °C / Inert atmosphere; Glovebox; Schlenk technique; Sealed tube 2: formic acid; [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); triethylamine / N,N-dimethyl-formamide / 23 °C / Inert atmosphere; Schlenk technique View Scheme
Multi-step reaction with 2 steps 1: bis(N-2,6-diisoprpylphenylbenzamidato)bis(dimethylamido)titanium (IV) / toluene / 14 h / 110 °C / Inert atmosphere; Glovebox; Schlenk technique; Sealed tube 2: formic acid; silver trifluoromethanesulfonate; [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); triethylamine / N,N-dimethyl-formamide / 16 h / 23 °C / Inert atmosphere; Schlenk technique View Scheme

: 74571-98-5
(3R)-3-methyl-4-(phenylmethyl)morpholine

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal at 80℃; under 45600 - 60800 Torr; for 2h;
With hydrogen; palladium 10% on activated carbon In ethanol under 2585.81 Torr;
With hydrogen; hydrogenchloride; palladium 10% on activated carbon In 1,4-dioxane; ethyl acetate under 2068.65 Torr; for 18h;

: 74571-95-2
(R)-2-[Benzyl-(2-hydroxy-ethyl)-amino]-propan-1-ol

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 70percent H2SO4 / 15 h / 140 °C 2: H2 / 10percent Pd/C / 2 h / 80 °C / 45600 - 60800 Torr View Scheme

: 1445590-35-1
(R)-2-bromo-N-(1-hydroxypropan-2-yl)-N-(4-methoxybenzyl)acetamide

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: sodium hydride / tetrahydrofuran / 25 °C / Inert atmosphere 2: lithium aluminium tetrahydride / tetrahydrofuran / Inert atmosphere; Reflux 3: palladium on activated charcoal; hydrogen / methanol / 18 h / 50 °C / 9500.64 Torr View Scheme

: 570398-22-0
(R)-4-(4-methoxybenzyl)-5-methylmorpholin-3-one

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: lithium aluminium tetrahydride / tetrahydrofuran / Inert atmosphere; Reflux 2: palladium on activated charcoal; hydrogen / methanol / 18 h / 50 °C / 9500.64 Torr View Scheme

: 42185-06-8
3-methylmorpholine

: C14H15NO4

A: C8H15NO2

B: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
In dichloromethane at 23℃; Inert atmosphere;

...Expand

: 1057322-63-0
2-chloro-N-(2-hydroxy-1-methyl-ethyl)-acetamide

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: potassium tert-butylate / dichloromethane; isopropyl alcohol / 1 h / 0 - 20 °C 2: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / 0 - 20 °C View Scheme

: C5H9NO

A: 350595-57-2
(S)-3-methylmorpholine

B: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
With [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); formic acid; silver trifluoromethanesulfonate; triethylamine In N,N-dimethyl-formamide at 23℃; for 16h; Inert atmosphere; Schlenk technique; enantioselective reaction;	A n/a B n/a

: C5H9NO

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
With [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); formic acid; triethylamine In N,N-dimethyl-formamide at 23℃; Reagent/catalyst; Inert atmosphere; Schlenk technique; enantioselective reaction;	n/a

: 634926-63-9
N-(tert-butyloxycarbonyl)-2-(propargyloxy)aminoethane

: 74572-04-6
(3R)-3-methylmorpholine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: methanol / 0 - 23 °C 2: bis(N-2,6-diisoprpylphenylbenzamidato)bis(dimethylamido)titanium (IV) / toluene / 14 h / 110 °C / Inert atmosphere; Glovebox; Schlenk technique; Sealed tube 3: formic acid; [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); triethylamine / N,N-dimethyl-formamide / 23 °C / Inert atmosphere; Schlenk technique View Scheme
Multi-step reaction with 3 steps 1: methanol / 0 - 23 °C 2: bis(N-2,6-diisoprpylphenylbenzamidato)bis(dimethylamido)titanium (IV) / toluene / 14 h / 110 °C / Inert atmosphere; Glovebox; Schlenk technique; Sealed tube 3: formic acid; silver trifluoromethanesulfonate; [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); triethylamine / N,N-dimethyl-formamide / 16 h / 23 °C / Inert atmosphere; Schlenk technique View Scheme

Yield

Multi-step reaction with 3 steps
1: methanol / 0 - 23 °C
2: bis(N-2,6-diisoprpylphenylbenzamidato)bis(dimethylamido)titanium (IV) / toluene / 14 h / 110 °C / Inert atmosphere; Glovebox; Schlenk technique; Sealed tube
3: formic acid; [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); triethylamine / N,N-dimethyl-formamide / 23 °C / Inert atmosphere; Schlenk technique
View Scheme

Multi-step reaction with 3 steps
1: methanol / 0 - 23 °C
2: bis(N-2,6-diisoprpylphenylbenzamidato)bis(dimethylamido)titanium (IV) / toluene / 14 h / 110 °C / Inert atmosphere; Glovebox; Schlenk technique; Sealed tube
3: formic acid; silver trifluoromethanesulfonate; [(1S,2S)-N-(p-toluensulfonyl)-1,2-diphenylethanediamine](p-cymene)ruthenium (I); triethylamine / N,N-dimethyl-formamide / 16 h / 23 °C / Inert atmosphere; Schlenk technique
View Scheme

: 6299-25-8
4,6-Dichloro-2-(methylthio)pyrimidine

: 74572-04-6
(3R)-3-methylmorpholine

: (3R)-4-[6-chloro-2-(methylsulfanyl)pyrimidin-4-yl]-3-methylmorpholine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 40℃; for 16h;	99%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 40℃;	68.1%

: 3,6-di-bromo-isothiazolo[4,3-b]pyridine

: 74572-04-6
(3R)-3-methylmorpholine

: (R)-4-(6-bromoisothiazolo[4,3-b]pyridin-3-yl)-3-methylmorpholine

Conditions

Conditions	Yield
In ethanol Reflux;	97%

: 1257236-41-1
2-chloro-N-methyl-N-(6-(2-morphplino-4-oxo-4H-chromen-8-yl)dibenzo[b,d]thiophen-2-yl)acetamide

: 74572-04-6
(3R)-3-methylmorpholine

: 1257234-75-5
N-methyl-2-[(3R)-3-methylmorpholin-4-yl]-N-[6-(2-morpholino-4-oxo-4H-chromen-8-yl)dibenzo[b,d]thiophen-2-yl]acetamide

Conditions

Conditions	Yield
With triethylamine In dichloromethane; ISOPROPYLAMIDE at 60℃; for 2h;	95%

: 1445591-92-3
(1R,2R)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentanecarboxylic acid

: 74572-04-6
(3R)-3-methylmorpholine

: 1445590-41-9
((1R,2R)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((R)-3-methylmorpholino)methanone

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane at 0 - 20℃; for 2h;	95%

: 1445592-12-0
(1R,2R)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-methoxycyclopentanecarboxylic acid

: 74572-04-6
(3R)-3-methylmorpholine

: 1445590-87-3
((1R,2R)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)-4-methoxycyclopentyl)((R)-3-methylmorpholino)methanone

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane at 20℃; for 2h;	95%

: 74572-04-6
(3R)-3-methylmorpholine

: 75-36-5
acetyl chloride

: 1257237-31-2
1-[(3R)-3-methylmorpholin-4-yl]ethan-1-one

Conditions

Conditions	Yield
Stage #1: (3R)-3-methylmorpholine With potassium carbonate In dichloromethane at 20℃; for 0.5h; Stage #2: acetyl chloride In dichloromethane at 20℃; for 18h;	95%
Stage #1: (3R)-3-methylmorpholine With potassium carbonate In dichloromethane at 0℃; for 0.5h; Stage #2: acetyl chloride In dichloromethane at 25℃; for 16h;	88%
Stage #1: (3R)-3-methylmorpholine With potassium carbonate In dichloromethane at 20℃; for 0.5h; Stage #2: acetyl chloride In dichloromethane at 20℃; for 18h;

: 19371-31-4
2,4-dichloro-6-piperidin-1-yl-[1,3,5]triazine

: 74572-04-6
(3R)-3-methylmorpholine

: 2-chloro-4-[(3R)-3-methylmorpholin-4-yl]-6-(piperidin-1-yl)-1,3,5-triazine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In 1,4-dioxane; dichloromethane at 20℃;	95%

: 1260585-63-4
(8S)-2-chloro-3-fluoro-8-(trifluoromethyl)-6,7,8,9-tetrahydro-4H-pyrimido[1,2-a]pyrimidin-4-one

: 74572-04-6
(3R)-3-methylmorpholine

: 1523412-61-4
(2S)-7-fluoro-8-[(3R)-3-methylmorpholin-4-yl]-2-(trifluoromethyl)-1,2,3,4-tetrahydropyrimido[1,2-a]pyrimidin-6-one

Conditions

Conditions	Yield
at 100℃; for 18h;	91%

: 6601-22-5
2,6-Dichloro-4-morpholino-1,3,5-triazine

: 74572-04-6
(3R)-3-methylmorpholine

: 2-chloro-4-[(3R)-3-methylmorpholin-4-yl]-6-(morpholin-4-yl)-1,3,5-triazine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In ethanol at 0 - 20℃; Suzuki Coupling;	91%
With N-ethyl-N,N-diisopropylamine In ethanol at 0 - 20℃;	91%
With N-ethyl-N,N-diisopropylamine In ethanol at 0 - 20℃;
With N-ethyl-N,N-diisopropylamine

: 108-77-0
1,3,5-trichloro-2,4,6-triazine

: 74572-04-6
(3R)-3-methylmorpholine

: (3R,3′R)-4,4′-(6-chloro-1,3,5-triazine-2,4-diyl)bis(3-methylmorpholine)

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃;	91%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃;	91%
In dichloromethane at 0 - 20℃;

: 74572-04-6
(3R)-3-methylmorpholine

: 90415-38-6
2,4-dichloro-6-(4-nitrophenyl)-1,3,5-triazine

: (R)-4-(4-chloro-6-(4-nitrophenyl)-1,3,5-triazin-2-yl)-3-methylmorpholine

Conditions

Conditions	Yield
With sodium hydrogencarbonate In water; acetone at 0 - 20℃; for 20h;	90%

: 3-(2,6-difluoropyridin-4-yl)-4-methylaniline

: 74572-04-6
(3R)-3-methylmorpholine

: (R)-3-(2-fluoro-6-(3-methylmorpholino)pyridin-4-yl)-4-methylaniline

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dimethyl sulfoxide at 100℃; for 18h;	90%

: 74572-04-6
(3R)-3-methylmorpholine

: 56844-12-3
6-bromo-4-chlorothieno[2,3-d]pyrimidine

: (R)-4-(6-bromothieno[2,3-d]pyrimidin-4-yl)-3-methylmorpholine

Conditions

Conditions	Yield
With triethylamine In 1,4-dioxane at 100℃;	88%

: 2,6-dichloropyrimidine-4-carbonitrile

: 74572-04-6
(3R)-3-methylmorpholine

: 2-chloro-6-[(3R)-3-methylmorpholin-4-yl]pyrimidine-4-carbonitrile

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; for 1.5h;	87.47%

: (3R,5S)-4-(4,6-dichloro-1,3,5-triazin-2-yl)-3,5-dimethylmorpholine

: 74572-04-6
(3R)-3-methylmorpholine

: (3R,5S)-4-(4-chloro-6-((R)-3-methylmorpholino)-1,3,5-triazin-2-yl)-3,5-dimethylmorpholine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0 - 20℃;	87%

: 16492-28-7
2,6-dichloro-4-pyrimidinecarboxylic acid

: 74572-04-6
(3R)-3-methylmorpholine

: 1233339-69-9
methyl 2-chloro-6-[(3R)-3-methylmorpholin-4-yl]pyrimidine-4-carboxylate

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; for 18h;	86%

: 74572-04-6
(3R)-3-methylmorpholine

: 6299-85-0
2,6-dichloropyrimidine-4-carboxylic acid methyl ester

: 1233339-69-9
methyl 2-chloro-6-[(3R)-3-methylmorpholin-4-yl]pyrimidine-4-carboxylate

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 20℃; for 18h;	86%
With triethylamine In dichloromethane at 20℃; for 18h;	79.19%
With triethylamine In dichloromethane at 20℃; for 16h; Temperature;	70%
With triethylamine In dichloromethane at 20℃; for 18h; Inert atmosphere;	9%

: 2897-43-0
2,6-dichloro-3-nitropyridin-4-amine

: 74572-04-6
(3R)-3-methylmorpholine

: (R)-6-chloro-2-(3-methylmorpholino)-3-nitropyridin-4-amine

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl acetamide at 80℃; for 3h;	86%

: 108-86-1
bromobenzene

: 74572-04-6
(3R)-3-methylmorpholine

: (R)-3-methyl-4-phenylmorpholine

Conditions

Conditions	Yield
With bis(tri-tert-butylphasphine)palladium dichloride; potassium tert-butylate In toluene for 3h; Reflux;	84%
With copper(l) iodide; potassium carbonate; L-proline In dimethyl sulfoxide at 90℃; for 24h;	5%

: 74572-04-6
(3R)-3-methylmorpholine

: 98-59-9
p-toluenesulfonyl chloride

: 1438397-95-5
(R)-3-methyl-4-tosylmorpholine

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃;	83%
With triethylamine In dichloromethane at 0 - 23℃;

: 74572-04-6
(3R)-3-methylmorpholine

: 136-72-1
piperic acid

: (2E,4E)-5-(benzo[d][1,3]dioxol-5-yl)-1-((R)-3-methylmorpholino)penta-2,4-dien-1-one

Conditions

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 8h;	83%

: (1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentanecarboxylic acid hydrochloride

: 74572-04-6
(3R)-3-methylmorpholine

: 1445590-70-4
((1S,2S)-2-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopentyl)((R)-3-methylmorpholino)methanone

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane at 20℃; for 2h;	82%

: 3764-01-0
2,4,6-trichloropyrimidine

: 74572-04-6
(3R)-3-methylmorpholine

: (3R)-4-(2,6-dichloropyrimidin-4-yl)-3-methylmorpholine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In ethanol at 65℃; for 12h; Cooling with ice;	81.2%
With triethylamine In ethanol at 20℃; for 16h;	71%
With triethylamine In ethanol at 20℃; for 16h;	71%

: 2,4-dichloro-6-((methylsulfonyl)methyl)pyrimidine

: 74572-04-6
(3R)-3-methylmorpholine

: 1233339-73-5
(R)-4-(2-chloro-6-(methylsulfonylmethyl)pyrimidin-4-yl)-3-methylmorpholine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 18h;	81%

: 13479-88-4
5,7-dichloro-[1,3]thiazolo[5,4-d]pyrimidine

: 74572-04-6
(3R)-3-methylmorpholine

: (R)-4-(5-chlorothiazolo[5,4-d]pyrimidin-7-yl)-3-methylmorpholine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In isopropyl alcohol at 20℃; for 1.5h; Inert atmosphere;	80%

: ethyl 2-(4-formylphenyl)thiazole-4-carboxylate

: 74572-04-6
(3R)-3-methylmorpholine

: (R)-2-(4-((3-methylmorpholine)methyl)phenyl)thiazole-4-carboxylic acid ethyl ester

Conditions

Conditions	Yield
Stage #1: ethyl 2-(4-formylphenyl)thiazole-4-carboxylate; (3R)-3-methylmorpholine In dichloromethane at 20 - 30℃; for 0.5h; Inert atmosphere; Stage #2: With sodium tris(acetoxy)borohydride In dichloromethane at 30℃; for 16h; Cooling with ice;	77.3%

: 108-77-0
1,3,5-trichloro-2,4,6-triazine

: 74572-04-6
(3R)-3-methylmorpholine

: 2,4-dichloro-6-[(3R)-3-methylmorpholin-4-yl]-1,3,5-triazine

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at -50℃; for 2h;	76%
With N-ethyl-N,N-diisopropylamine In dichloromethane at -50℃; for 2h;	76%
With N-ethyl-N,N-diisopropylamine In dichloromethane at -50℃; for 10h;

: 4316-93-2
4,6-dichloro-5-nitropyrimidine

: 74572-04-6
(3R)-3-methylmorpholine

: (R)-4-(6-chloro-5-nitropyrimidin-4-yl)-3-methylmorpholine

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 0℃; for 0.5h;	75%

(R)-3-Methylmorpholine Specification

The cas register number of (R)-3-Methylmorpholine is 74572-04-6. It also can be called as Morpholine,3-methyl-, (3R)- and the Systematic name about this chemical is Morpholine,3-methyl-, (3R)-.

Physical properties about (R)-3-Methylmorpholine are: (1)ACD/LogP: -0.59; (2)ACD/LogD (pH 5.5): -3.55; (3)ACD/LogD (pH 7.4): -2.22; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 1; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 2; (9)#H bond donors: 1; (10)Polar Surface Area: 12.47Å²; (11)Index of Refraction: 1.409; (12)Molar Refractivity: 28.1 cm³; (13)Molar Volume: 113.5 cm³; (14)Polarizability: 11.14x10^-24cm³; (15)Surface Tension: 26.2 dyne/cm; (16)Enthalpy of Vaporization: 37.45 kJ/mol; (17)Vapour Pressure: 7.14 mmHg at 25°C.

You can still convert the following datas into molecular structure:
(1)SMILES: O1C[C@H](NCC1)C
(2)InChI: InChI=1/C5H11NO/c1-5-4-7-3-2-6-5/h5-6H,2-4H2,1H3/t5-/m1/s1
(3)InChIKey: SFWWGMKXCYLZEG-RXMQYKEDBJ
(4)Std. InChI: InChI=1S/C5H11NO/c1-5-4-7-3-2-6-5/h5-6H,2-4H2,1H3/t5-/m1/s1
(5)Std. InChIKey: SFWWGMKXCYLZEG-RXMQYKEDSA-N

Product Name

(R)-3-Methylmorpholine

Synthetic route

(R)-3-Methylmorpholine Specification

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