Product Name

  • Name

    4-(3-chloropropyl)morpholinium chloride

  • EINECS 260-851-0
  • CAS No. 57616-74-7
  • Article Data11
  • CAS DataBase
  • Density
  • Solubility
  • Melting Point 164-166 °C
  • Formula C7H14ClNO.HCl
  • Boiling Point 227.1 °C at 760 mmHg
  • Molecular Weight 200.108
  • Flash Point 91.2 °C
  • Transport Information
  • Appearance
  • Safety 26-36/37/39-45
  • Risk Codes 21-25-34-43
  • Molecular Structure Molecular Structure of 57616-74-7 (4-(3-chloropropyl)morpholinium chloride)
  • Hazard Symbols T
  • Synonyms Morpholine,4-(3-chloropropyl)-, hydrochloride (6CI,7CI,9CI);3-(Morpholino)propyl chloridehydrochloride;Morpholinopropylchloride hydrochloride;N-(3-Chloropropyl)morpholine hydrochloride;
  • PSA 12.47000
  • LogP 1.68740

Synthetic route

morpholine
110-91-8

morpholine

1,3-chlorobromopropane
109-70-6

1,3-chlorobromopropane

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

Conditions
ConditionsYield
Stage #1: morpholine; 1.3-chlorobromopropane In toluene at 84℃; for 3h;
Stage #2: With hydrogenchloride In 1,4-dioxane; toluene		90%
Stage #1: morpholine; 1.3-chlorobromopropane In toluene at 84℃; for 3h;
Stage #2: With hydrogenchloride In 1,4-dioxane		90%
Stage #1: morpholine; 1.3-chlorobromopropane In toluene at 84℃; for 3h;
Stage #2: With hydrogenchloride In 1,4-dioxane		90%
morpholine
110-91-8

morpholine

1-iodo-3-chloro-propane
6940-76-7

1-iodo-3-chloro-propane

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

Conditions
ConditionsYield
Stage #1: morpholine; 1-iodo-3-chloro-propane With potassium carbonate In N,N-dimethyl-formamide for 16h;
Stage #2: With hydrogenchloride In 1,4-dioxane; diethyl ether		32%
5-hydroxy-4-methoxy-2-nitrobenzoic acid ethyl ester
1146162-38-0

5-hydroxy-4-methoxy-2-nitrobenzoic acid ethyl ester

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

ethyl 4-methoxy-5-(3-morpholin-4-ylpropoxy)-2-nitrobenzoate
1040264-48-9

ethyl 4-methoxy-5-(3-morpholin-4-ylpropoxy)-2-nitrobenzoate

Conditions
ConditionsYield
With potassium carbonate In 1,4-dioxane for 7h; Product distribution / selectivity; Reflux;98%
methyl 2-nitro-4-methoxy-5-hydroxybenzoate
215659-03-3

methyl 2-nitro-4-methoxy-5-hydroxybenzoate

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

4-methoxy-5-(3-morpholinylpropoxy)-2-nitrobenzoic acid methyl ester
214472-37-4

4-methoxy-5-(3-morpholinylpropoxy)-2-nitrobenzoic acid methyl ester

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 2.5h; Reflux;87.5%
With potassium carbonate In acetonitrile for 2.5h; Reflux;
2-sulfanylidene-2,3-dihydropyrazolo[1,5-a][1,3,5]triazin-4(1H)-one
34682-99-0

2-sulfanylidene-2,3-dihydropyrazolo[1,5-a][1,3,5]triazin-4(1H)-one

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

2-(2-(morpholinyl)ethylthio)-3H-pyrazolo[1,5-a][1,3,5]triazin-4-one

2-(2-(morpholinyl)ethylthio)-3H-pyrazolo[1,5-a][1,3,5]triazin-4-one

Conditions
ConditionsYield
With potassium iodide; sodium hydroxide In methanol; water at 20℃; for 4h;87%
5-amino-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-8-ol
1032570-71-0

5-amino-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-8-ol

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine
1032570-74-3

7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine

Conditions
ConditionsYield
In water; N,N-dimethyl-formamide at 90℃; for 5h; Solvent; Large scale;86%
1-(2-fluoro-4-nitrophenyl)-6-hydroxy-7-methoxy-quinoline
479690-08-9

1-(2-fluoro-4-nitrophenyl)-6-hydroxy-7-methoxy-quinoline

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

4-(3-((4-(2-fluoro-4-nitrophenoxy)-6-methoxyquinolin-7-yl)oxy)propyl)morpholine
960299-44-9

4-(3-((4-(2-fluoro-4-nitrophenoxy)-6-methoxyquinolin-7-yl)oxy)propyl)morpholine

Conditions
ConditionsYield
With caesium carbonate; potassium iodide In acetonitrile at 20℃; for 3.75h; Reflux;83%
2-(4-nitrophenyl)imidazo[1,2-a]pyridin-6-ol

2-(4-nitrophenyl)imidazo[1,2-a]pyridin-6-ol

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

4-(3-((2-(4-nitrophenyl)imidazo[1,2-a]pyridin-6-yl)oxy)propyl)morpholine

4-(3-((2-(4-nitrophenyl)imidazo[1,2-a]pyridin-6-yl)oxy)propyl)morpholine

Conditions
ConditionsYield
With tetra-(n-butyl)ammonium iodide; potassium carbonate In N,N-dimethyl-formamide for 6h; Reflux;80%
N-(8-hydroxy-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)nicotinamide bis(trifluoroacetate)

N-(8-hydroxy-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)nicotinamide bis(trifluoroacetate)

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

N-{7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl}nicotinamide
1032570-54-9

N-{7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl}nicotinamide

Conditions
ConditionsYield
Stage #1: N-(8-hydroxy-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl)nicotinamide bis(trifluoroacetate) With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 1.5h;
Stage #2: N-(3-chloropropyl)morpholine hydrochloride In N,N-dimethyl-formamide at 60℃; for 20h;		79%
N-{3-fluoro-4-[(7-hydroxy-6-methoxyquinolin-4-yl)oxy]phenyl}-N'-(2-phenylethyl)ethanediamide

N-{3-fluoro-4-[(7-hydroxy-6-methoxyquinolin-4-yl)oxy]phenyl}-N'-(2-phenylethyl)ethanediamide

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

N-(3-fluoro-4-{[6-methoxy-7-(3-morpholin-4-ylpropoxy)quinolin-4-yl]oxy}phenyl)-N'-(2-phenylethyl)ethanediamide

N-(3-fluoro-4-{[6-methoxy-7-(3-morpholin-4-ylpropoxy)quinolin-4-yl]oxy}phenyl)-N'-(2-phenylethyl)ethanediamide

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃;74%
With potassium carbonate In N,N-dimethyl-formamide at 80℃;74%
N-[3-fluoro-4-[[7-hydroxy-6-methoxy-quinolin-4-yl]oxy]phenyl]-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide
849217-50-1

N-[3-fluoro-4-[[7-hydroxy-6-methoxy-quinolin-4-yl]oxy]phenyl]-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

foretinib
849217-64-7

foretinib

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 5h;72%
4-hydroxy-3-phenylcoumarin
1786-05-6

4-hydroxy-3-phenylcoumarin

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

4-(3-morpholin-4-yl-propoxy)-3-phenyl-chromen-2-one
64555-45-9

4-(3-morpholin-4-yl-propoxy)-3-phenyl-chromen-2-one

Conditions
ConditionsYield
71%
4,5-diphenyl-1H-imidazole
668-94-0

4,5-diphenyl-1H-imidazole

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

4-[3-(4,5-diphenylimidazol-1-yl)-propyl]morpholine
473826-15-2

4-[3-(4,5-diphenylimidazol-1-yl)-propyl]morpholine

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 24h; Heating / reflux;68%
5-nitroguaiacol
636-93-1

5-nitroguaiacol

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

4-[3-(2-methoxy-5-nitrophenoxy)propyl]morpholine
1292318-17-2

4-[3-(2-methoxy-5-nitrophenoxy)propyl]morpholine

Conditions
ConditionsYield
With caesium carbonate; sodium iodide In N,N-dimethyl-formamide at 110℃; for 16h;61%
N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

3-butyryl-4-(2-methylphenylamino)-8-hydroxyquinoline
125500-46-1

3-butyryl-4-(2-methylphenylamino)-8-hydroxyquinoline

3-butyryl-4-(2-methylphenylamino)-8-(3-morpholinopropoxy)quinoline

3-butyryl-4-(2-methylphenylamino)-8-(3-morpholinopropoxy)quinoline

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 100℃; for 2.5h;58%
ethyl 3,4-bis(benzyloxy)-5-(dimethylcarbamoyl)-1-(4-hydroxyphenyl)-1H-pyrrole-2-carboxylate
1443300-48-8

ethyl 3,4-bis(benzyloxy)-5-(dimethylcarbamoyl)-1-(4-hydroxyphenyl)-1H-pyrrole-2-carboxylate

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

ethyl 3,4-bis(benzyloxy)-5-(dimethylcarbamoyl)-1-(4-(3-morpholinopropoxy)phenyl)-1H-pyrrole-2-carboxylate
1443300-49-9

ethyl 3,4-bis(benzyloxy)-5-(dimethylcarbamoyl)-1-(4-(3-morpholinopropoxy)phenyl)-1H-pyrrole-2-carboxylate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 18h;57%
(cis)-1-(1H-benzimidazol-2-ylmethyl)-1,2,3,4,4a,5,6,10b-octahydro-1,10-phenanthroline

(cis)-1-(1H-benzimidazol-2-ylmethyl)-1,2,3,4,4a,5,6,10b-octahydro-1,10-phenanthroline

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

(cis)-1-({1-[3-(4-morpholinyl)propyl]-1H-benzimidazol-2-yl}methyl)-1,2,3,4,4a,5,6,10b-octahydro-1,10-phenanthroline

(cis)-1-({1-[3-(4-morpholinyl)propyl]-1H-benzimidazol-2-yl}methyl)-1,2,3,4,4a,5,6,10b-octahydro-1,10-phenanthroline

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 80℃; for 16h;56%
5-{[(3-hydroxy-4-methoxyphenyl)amino]methylene}-2,2-dimethyl-1,3-dioxane-4,6-dione
205448-27-7

5-{[(3-hydroxy-4-methoxyphenyl)amino]methylene}-2,2-dimethyl-1,3-dioxane-4,6-dione

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

5-((3-(3-morpholinopropoxy)-4-methoxyanilino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione
205448-37-9

5-((3-(3-morpholinopropoxy)-4-methoxyanilino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In DMF (N,N-dimethyl-formamide) at 60℃; for 2h;51%
5-amino-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-8-ol bis(trifluoroacetate)

5-amino-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-8-ol bis(trifluoroacetate)

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine
1032570-74-3

7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine

Conditions
ConditionsYield
Stage #1: 5-amino-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-8-ol bis(trifluoroacetate) With triethylamine In dichloromethane at 20℃; for 1.5h;
Stage #2: N-(3-chloropropyl)morpholine hydrochloride With caesium carbonate In N,N-dimethyl-formamide at 70 - 75℃; for 4.5h;		44%
methyl 4-bromo-1H-indazole-6-carboxylate
885518-47-8

methyl 4-bromo-1H-indazole-6-carboxylate

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

methyl 4-bromo-1-[3-(morpholin-4-yl)propyl]-1H-indazole-6-carboxylate

methyl 4-bromo-1-[3-(morpholin-4-yl)propyl]-1H-indazole-6-carboxylate

Conditions
ConditionsYield
With 18-crown-6 ether; sodium hexamethyldisilazane In tetrahydrofuran for 16h; Reflux; Inert atmosphere;43%
N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

N-[2-[[(tert-butylamino)carbonyl]amino]-3-(3,5-dimethoxyphenyl)-1,6-naphthyridin-7-yl]acetamide
311819-90-6

N-[2-[[(tert-butylamino)carbonyl]amino]-3-(3,5-dimethoxyphenyl)-1,6-naphthyridin-7-yl]acetamide

1-tert-butyl-3-[3-(3,5-dimethoxy-phenyl)-7-(3-morpholin-4-yl-propylamino)-[1,6]naphthyridin-2-yl]-urea

1-tert-butyl-3-[3-(3,5-dimethoxy-phenyl)-7-(3-morpholin-4-yl-propylamino)-[1,6]naphthyridin-2-yl]-urea

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide at 52℃; for 26h;41%
6-(4-hydroxyphenyl)-3,9-dimethoxy-5H-indeno[1,2-c] isoquinoline-5,11(6H)-diketone
1225021-05-5

6-(4-hydroxyphenyl)-3,9-dimethoxy-5H-indeno[1,2-c] isoquinoline-5,11(6H)-diketone

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

3,9-dimethoxy-6-(4-(3-morpholinopropoxy)phenyl)-5H-indeno[1,2-c]isoquinoline-5,11(6H)-dione

3,9-dimethoxy-6-(4-(3-morpholinopropoxy)phenyl)-5H-indeno[1,2-c]isoquinoline-5,11(6H)-dione

Conditions
ConditionsYield
Stage #1: 6-(4-hydroxyphenyl)-3,9-dimethoxy-5H-indeno[1,2-c] isoquinoline-5,11(6H)-diketone; N-(3-chloropropyl)morpholine hydrochloride With tetrabutylammomium bromide In tetrahydrofuran at 20℃;
Stage #2: With sodium hydroxide In tetrahydrofuran; water for 4h; Reflux; Inert atmosphere;		38%
formic acid
64-18-6

formic acid

3-Bromophenol
591-20-8

3-Bromophenol

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

4-(3-(3-bromophenoxy)propyl)morpholine formic acid salt

4-(3-(3-bromophenoxy)propyl)morpholine formic acid salt

Conditions
ConditionsYield
Stage #1: 3-Bromophenol; N-(3-chloropropyl)morpholine hydrochloride With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 40℃; for 88h;
Stage #2: formic acid		38%
...Expand
C29H25F2N3O5

C29H25F2N3O5

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

(2R,3R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N-(4-fluorophenyl)-2,3-dimethylcyclopropane-1,1-dicarboxamide hydrochloride
1035375-43-9

(2R,3R)-N-[3-fluoro-4-({6-(methyloxy)-7-[(3-morpholin-4-ylpropyl)oxy]quinolin-4-yl}oxy)phenyl]-N-(4-fluorophenyl)-2,3-dimethylcyclopropane-1,1-dicarboxamide hydrochloride

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 4h;37%
4-[2-(diethylamino)ethoxy]-2-(4-propoxyphenyl)quinolin-6-ol

4-[2-(diethylamino)ethoxy]-2-(4-propoxyphenyl)quinolin-6-ol

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

N,N-diethyl-2-{[6-(3-morpholin-4-ylpropoxy)-2-(4-propoxyphenyl)quinolin-4-yl]oxy}ethanamine

N,N-diethyl-2-{[6-(3-morpholin-4-ylpropoxy)-2-(4-propoxyphenyl)quinolin-4-yl]oxy}ethanamine

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 2h; Inert atmosphere;37%
2-(3-aminophenyl-(4-methoxybenzyl)-amino)-N-(1,7,7-trimethylbicyclo[2.2.1]heptan-endo-2-yl)pyrimidine-4-carboxamide

2-(3-aminophenyl-(4-methoxybenzyl)-amino)-N-(1,7,7-trimethylbicyclo[2.2.1]heptan-endo-2-yl)pyrimidine-4-carboxamide

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

2-((4-methoxybenzyl)-(3-(3-morpholinopropylamino)phenyl)amino)-N-(1,7,7-trimethylbicyclo[2.2.1]heptan-endo-2-yl)pyrimidine-4-carboxamide

2-((4-methoxybenzyl)-(3-(3-morpholinopropylamino)phenyl)amino)-N-(1,7,7-trimethylbicyclo[2.2.1]heptan-endo-2-yl)pyrimidine-4-carboxamide

Conditions
ConditionsYield
With potassium hydrogencarbonate; potassium iodide In 2-ethoxy-ethanol at 110℃; for 2.5h;36%
N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

(3-Bromo-phenyl)-(8H-pyrrolo[3,2-g]quinazolin-4-yl)-amine

(3-Bromo-phenyl)-(8H-pyrrolo[3,2-g]quinazolin-4-yl)-amine

5-[(3-bromophenyl)amino]-1-[3-(4-morpholino)propyl]pyrrolo[3,2-g]quinazoline

5-[(3-bromophenyl)amino]-1-[3-(4-morpholino)propyl]pyrrolo[3,2-g]quinazoline

Conditions
ConditionsYield
With 4 A molecular sieve In acetone Heating;34%
6-(4-hydroxyphenyl)-5H-indeno[1,2-c]isoquinoline-5,11(6H)-diketone
1225021-03-3

6-(4-hydroxyphenyl)-5H-indeno[1,2-c]isoquinoline-5,11(6H)-diketone

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

6-(4-(3-morpholinylpropoxy) phenyl)-5H-indeno[1,2-c]isoquinoline-5,11(6H)diketone
1225020-94-9

6-(4-(3-morpholinylpropoxy) phenyl)-5H-indeno[1,2-c]isoquinoline-5,11(6H)diketone

Conditions
ConditionsYield
With potassium carbonate In acetone for 12h; Reflux;32%
4-((2,4-difluorophenyl)amino)-7-methoxyquinazolin-6-ol
184475-74-9

4-((2,4-difluorophenyl)amino)-7-methoxyquinazolin-6-ol

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

4-[(2,4-difluorophenyl)amino]-6-[3-(morpholin-4-yl)propyloxy]-7-methoxyquinazoline

4-[(2,4-difluorophenyl)amino]-6-[3-(morpholin-4-yl)propyloxy]-7-methoxyquinazoline

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide30%
4-(2-piperidin-1-ylethoxy)-2-(4-propoxyphenyl)quinolin-6-ol

4-(2-piperidin-1-ylethoxy)-2-(4-propoxyphenyl)quinolin-6-ol

N-(3-chloropropyl)morpholine hydrochloride
57616-74-7

N-(3-chloropropyl)morpholine hydrochloride

C32H43N3O4

C32H43N3O4

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 90℃; for 2h; Inert atmosphere;18%

4-(3-Chloropropyl)morpholine hydrochloride Specification

The 4-(3-Chloropropyl)morpholine hydrochloride, with the CAS registry number 57616-74-7, is also known as Morpholinopropylchloride hydrochloride. Its EINECS number is 260-851-0. This chemical's molecular formula is C7H14ClNO.HCl and molecular weight is 200.11. What's more, its systematic name is 4-(3-Chloropropyl)morpholin-4-ium chloride.

Physical properties of 4-(3-Chloropropyl)morpholine hydrochloride are: (1)ACD/LogP: 0.656; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.19; (4)ACD/LogD (pH 7.4): 0.37; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 1.00; (8)ACD/KOC (pH 7.4): 28.11; (9)#H bond acceptors: 2; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 9.23 Å2; (13)Flash Point: 91.2 °C; (14)Enthalpy of Vaporization: 46.37 kJ/mol; (15)Boiling Point: 227.1 °C at 760 mmHg; (16)Vapour Pressure: 0.0789 mmHg at 25°C.

You can still convert the following datas into molecular structure:
(1)SMILES: [Cl-].ClCCC[NH+]1CCOCC1
(2)Std. InChI: InChI=1S/C7H14ClNO.ClH/c8-2-1-3-9-4-6-10-7-5-9;/h1-7H2;1H
(3)Std. InChIKey: PQECODMSWJOUAT-UHFFFAOYSA-N

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