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123-00-2

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123-00-2 Usage

Chemical Properties

Clear liquid

Uses

Different sources of media describe the Uses of 123-00-2 differently. You can refer to the following data:
1. Fiber synthesis; chemical intermediate.
2. 3-(4-Morpholinyl)propylamine is catalytic agent, petrochemical additive. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.

Definition

ChEBI: A member of the class of morpholines that is morpholine substituted by a 3-aminopropyl group a the N atom.

General Description

A colorless liquid with a faint, fishlike odor. Burns, but requires some effort to ignite. Corrosive to tissue. Produces toxic oxides of nitrogen during combustion.

Air & Water Reactions

Soluble in water.

Reactivity Profile

N-(3-Aminopropyl)morpholine behaves as an amine. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.

Hazard

Strongly irritant to tissue.

Health Hazard

TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Safety Profile

A corrosive material. Moderately toxic by several routes. A severe skin and eye irritant. Combustible. Can react with oxidizing materials. To fight fire, use alcohol foam, dry chemical. When heated to decomposition it emits toxic fumes of NOx,.

Check Digit Verification of cas no

The CAS Registry Mumber 123-00-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123-00:
(5*1)+(4*2)+(3*3)+(2*0)+(1*0)=22
22 % 10 = 2
So 123-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O/c1-2-7(8)9-3-5-10-6-4-9/h7H,2-6,8H2,1H3

123-00-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B23485)  3-(4-Morpholinyl)propylamine, 98%   

  • 123-00-2

  • 50g

  • 390.0CNY

  • Detail
  • Alfa Aesar

  • (B23485)  3-(4-Morpholinyl)propylamine, 98%   

  • 123-00-2

  • 250g

  • 1622.0CNY

  • Detail
  • Aldrich

  • (A9028)  3-Morpholinopropylamine  Liquid

  • 123-00-2

  • A9028-100ML

  • 607.23CNY

  • Detail
  • Aldrich

  • (A9028)  3-Morpholinopropylamine  Liquid

  • 123-00-2

  • A9028-500ML

  • 2,303.73CNY

  • Detail

123-00-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-morpholinopropylamine

1.2 Other means of identification

Product number -
Other names 4-Morpholinepropanamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Functional fluids (closed systems),Intermediates,Pigments
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:123-00-2 SDS

123-00-2Synthetic route

2-Trimethylsilanyl-ethanesulfonic acid (3-morpholin-4-yl-propyl)-amide
106018-95-5

2-Trimethylsilanyl-ethanesulfonic acid (3-morpholin-4-yl-propyl)-amide

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

Conditions
ConditionsYield
With cesium fluoride In N,N-dimethyl-formamide at 95℃; for 40h;90%
morpholine
110-91-8

morpholine

Argopore Wang resin-bound 3-amino-1-propanol

Argopore Wang resin-bound 3-amino-1-propanol

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

Conditions
ConditionsYield
Stage #1: Argopore Wang resin-bound 3-amino-1-propanol With 1H-imidazole; iodine; triphenylphosphine In N,N-dimethyl-formamide for 16h;
Stage #2: morpholine In N,N-dimethyl-formamide at 50℃; for 6h;
Stage #3: With trifluoroacetic acid In dichloromethane for 1h;
86%
2-(3-morpholinylpropyl)-1H-isoindole-1,3(2H)-dione
6820-95-7

2-(3-morpholinylpropyl)-1H-isoindole-1,3(2H)-dione

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

Conditions
ConditionsYield
With hydrazine hydrate In ethanol for 24h; Reflux;86%
With hydrazine hydrate In ethanol at 20℃; Reflux;85%
With hydrazine hydrate In ethanol Reflux;
With hydrazine hydrate In ethanol for 0.75h; Reflux;
With hydrazine hydrate In ethanol Reflux;
3-Morpholin-4-yl-propionitrile
4542-47-6

3-Morpholin-4-yl-propionitrile

A

morpholine
110-91-8

morpholine

B

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

Conditions
ConditionsYield
With sodium tetrahydroborate; hydrogen; nickel dichloride In tert-butyl alcohol at 70℃; under 760.051 Torr; for 8h;A 22%
B 59%
morpholine
110-91-8

morpholine

N-(3-chloropropyl)phthalimide
42251-84-3

N-(3-chloropropyl)phthalimide

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

Conditions
ConditionsYield
With xylene Erhitzen des Reaktionsprodukts mit konz. wss. HCl;
morpholine
110-91-8

morpholine

2-(3-bromopropyl)isoindole-1,3-dione
5460-29-7

2-(3-bromopropyl)isoindole-1,3-dione

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

Conditions
ConditionsYield
Erhitzen des Reaktionsprodukts mit wss. HCl;
3-(1-pyrrolidinyl)propylamine
23159-07-1

3-(1-pyrrolidinyl)propylamine

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

Conditions
ConditionsYield
With diazene In ethanol for 3h;
morpholine
110-91-8

morpholine

3-chloropropylamine hydrochloride
6276-54-6

3-chloropropylamine hydrochloride

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In acetonitrile at 30℃; for 8h;
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

2-methyl-pyridine-4-carbaldehyde
63875-01-4

2-methyl-pyridine-4-carbaldehyde

2-methylpyridine-4-carboxaldehyde [3-(4-morpholinyl)propyl]imine

2-methylpyridine-4-carboxaldehyde [3-(4-morpholinyl)propyl]imine

Conditions
ConditionsYield
With magnesium sulfate100%
With magnesium sulfate In toluene for 18h;
With magnesium sulfate
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

C17H17F3O3
938455-56-2

C17H17F3O3

di(succinimido) carbonate
74124-79-1

di(succinimido) carbonate

C25H31F3N2O5

C25H31F3N2O5

Conditions
ConditionsYield
Stage #1: C17H17F3O3; di(succinimido) carbonate With triethylamine In acetonitrile at 20℃; for 1h;
Stage #2: 4-(3-Aminopropyl)morpholine In acetonitrile at 20℃; for 0.25h; Further stages.;
100%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

5-methyl 2-(2-chloroethoxy)methyl-4-(3-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate
314034-08-7

5-methyl 2-(2-chloroethoxy)methyl-4-(3-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate

3-methyl-6-(2-chloroethoxy)methyl-4-(3-chlorophenyl)-2-methyl-5-(3-(N-morpholino)propylcarbamoyl)-1,4-dihydropyridine-3-carboxylate
314034-14-5

3-methyl-6-(2-chloroethoxy)methyl-4-(3-chlorophenyl)-2-methyl-5-(3-(N-morpholino)propylcarbamoyl)-1,4-dihydropyridine-3-carboxylate

Conditions
ConditionsYield
With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 20h;100%
In dichloromethane; ethyl acetate
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

4-iodobenzenesulfonyl chloride
98-61-3

4-iodobenzenesulfonyl chloride

N-(3-Morpholinopropyl)-4-iodobenzenesulphonamide
403793-23-7

N-(3-Morpholinopropyl)-4-iodobenzenesulphonamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 0.5h;100%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

ethyl 4-chloro-3-nitrobenzoate
16588-16-2

ethyl 4-chloro-3-nitrobenzoate

C16H23N3O5
310451-70-8

C16H23N3O5

Conditions
ConditionsYield
With triethylamine In ethanol at 60℃; for 12h;100%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

3-chloro-6,7,8,9-tetrahydronaphto[2,3-e][1,2,4]triazine 1-oxide
911299-74-6

3-chloro-6,7,8,9-tetrahydronaphto[2,3-e][1,2,4]triazine 1-oxide

N-[3-(4-morpholinyl)propyl]-6,7,8,9-tetrahydronaphto[2,3-e][1,2,4]triazin-3-amine 1-oxide

N-[3-(4-morpholinyl)propyl]-6,7,8,9-tetrahydronaphto[2,3-e][1,2,4]triazin-3-amine 1-oxide

Conditions
ConditionsYield
In 1,2-dimethoxyethane for 8h; Reflux;100%
In 1,2-dimethoxyethane for 0.5h; Heating / reflux;100%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

ethyl 2-acetyl-4-oxo-4-phenylbutanoate
52313-46-9

ethyl 2-acetyl-4-oxo-4-phenylbutanoate

ethyl 2-methyl-1-(3-morpholinopropyl)-5-phenyl-1H-pyrrole-3-carboxylate

ethyl 2-methyl-1-(3-morpholinopropyl)-5-phenyl-1H-pyrrole-3-carboxylate

Conditions
ConditionsYield
With 3-hydroxy-4-methylbenzenesulfonic acid In ethanol for 16h; Inert atmosphere; Reflux;100%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

1-(3,4-dichlorophenyl)-1H-1,2,3-triazole-4-carboxylic acid

1-(3,4-dichlorophenyl)-1H-1,2,3-triazole-4-carboxylic acid

N-(3-morpholinopropyl) 1-(3,4-dichlorophenyl)-1H-1,2,3-triazole-4-carboxamide

N-(3-morpholinopropyl) 1-(3,4-dichlorophenyl)-1H-1,2,3-triazole-4-carboxamide

Conditions
ConditionsYield
Stage #1: 1-(3,4-dichlorophenyl)-1H-1,2,3-triazole-4-carboxylic acid With 1,1'-carbonyldiimidazole In tetrahydrofuran for 2h; Reflux;
Stage #2: 4-(3-Aminopropyl)morpholine In tetrahydrofuran at 20℃;
100%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

3,4-diethoxy-3-cyclobuten-1,2-dione
5231-87-8

3,4-diethoxy-3-cyclobuten-1,2-dione

3-ethoxy-4-((3-morpholinopropyl)amino)cyclobut-3-ene-1,2-dione

3-ethoxy-4-((3-morpholinopropyl)amino)cyclobut-3-ene-1,2-dione

Conditions
ConditionsYield
In tetrahydrofuran at -78 - 20℃;100%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

oxalic acid diethyl ester
95-92-1

oxalic acid diethyl ester

N,N'-bis(3-dimethylaminopropyl)oxalamide
25148-90-7

N,N'-bis(3-dimethylaminopropyl)oxalamide

Conditions
ConditionsYield
In ethanol Inert atmosphere; Flow reactor;100%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

4-bromo-1,8-naphthalenedicarboxylic anhydride
81-86-7

4-bromo-1,8-naphthalenedicarboxylic anhydride

6-bromo-2-(3-morpholinopropyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione

6-bromo-2-(3-morpholinopropyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione

Conditions
ConditionsYield
In ethanol at 90℃; for 12h;99%
In ethanol at 60℃; for 6h;87%
In ethanol Reflux;78.4%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

(S)-11-cyclohexyl-4-ethyl-4-hydroxy-1,12-dihydro-14H-pyrano-[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H)-dione
78287-30-6

(S)-11-cyclohexyl-4-ethyl-4-hydroxy-1,12-dihydro-14H-pyrano-[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H)-dione

C33H42N4O5

C33H42N4O5

Conditions
ConditionsYield
at 60℃; Inert atmosphere;99%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

2,4-bis(3-formylphenyl)quinoline

2,4-bis(3-formylphenyl)quinoline

2,4-bis{3-[(3-morpholinopropyl)iminomethyl]phenyl}quinoline

2,4-bis{3-[(3-morpholinopropyl)iminomethyl]phenyl}quinoline

Conditions
ConditionsYield
In ethanol for 5h; Reflux;99%
N-[(E)-dimethylaminomethylideneamino]acetamide

N-[(E)-dimethylaminomethylideneamino]acetamide

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

4-(3-N-morpholine-propyl)-3-methyl-1,2,4-triazole

4-(3-N-morpholine-propyl)-3-methyl-1,2,4-triazole

Conditions
ConditionsYield
With acetic acid microwave irradiation;98%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

3-Chloro-7-methylbenzo-1,2,4-triazine 1-Oxide
54448-50-9

3-Chloro-7-methylbenzo-1,2,4-triazine 1-Oxide

7-methyl-N-[3-(4-morpholinyl)propyl]-1,2,4-benzotriazin-3-amine 1-oxide
763131-85-7

7-methyl-N-[3-(4-morpholinyl)propyl]-1,2,4-benzotriazin-3-amine 1-oxide

Conditions
ConditionsYield
In methanol; 1,2-dimethoxyethane98%
In 1,2-dimethoxyethane for 8h; Heating / reflux;98%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

3-chloro-7-methyl-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazine 1-oxide
911299-29-1

3-chloro-7-methyl-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazine 1-oxide

7-methyl-N-[3-(4-morpholinyl)propyl]-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-amine 1-oxide

7-methyl-N-[3-(4-morpholinyl)propyl]-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-amine 1-oxide

Conditions
ConditionsYield
With triethylamine In 1,2-dimethoxyethane for 8h; Reflux;98%
With triethylamine In 1,2-dimethoxyethane for 8h; Heating / reflux;98%
3-chloro-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-amine 1-oxide
910105-60-1

3-chloro-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-amine 1-oxide

4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

N-[3-(4-morpholinyl)propyl]-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-amine 1-oxide

N-[3-(4-morpholinyl)propyl]-7,8-dihydro-6H-indeno[5,6-e][1,2,4]triazin-3-amine 1-oxide

Conditions
ConditionsYield
In 1,2-dimethoxyethane for 8h; Reflux;98%
In 1,2-dimethoxyethane for 3h; Reflux;98%
In 1,2-dimethoxyethane for 3h; Heating / reflux;98%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

stearic acid
57-11-4

stearic acid

N-(3-morpholinopropyl) stearamide
55852-13-6

N-(3-morpholinopropyl) stearamide

Conditions
ConditionsYield
With nano sulfated-TiO2 at 115℃; under 760.051 Torr; for 1h; Neat (no solvent);98%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

2-chloro-N-(4-chlorophenyl)acetamide
3289-75-6

2-chloro-N-(4-chlorophenyl)acetamide

N-(4-chlorophenyl)-2-((3-morpholinopropyl)amino)acetamide

N-(4-chlorophenyl)-2-((3-morpholinopropyl)amino)acetamide

Conditions
ConditionsYield
With triethylamine In acetonitrile Reflux;98%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

2,4-bis(3-formylphenyl)quinazoline

2,4-bis(3-formylphenyl)quinazoline

2,4-bis{3-[(3-morpholinopropyl)iminomethyl]phenyl}quinazoline

2,4-bis{3-[(3-morpholinopropyl)iminomethyl]phenyl}quinazoline

Conditions
ConditionsYield
In ethanol for 5h; Reflux;98%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

2,4-bis(4-formylphenyl)quinoline

2,4-bis(4-formylphenyl)quinoline

2,4-bis{4-[(3-morpholinopropyl)iminomethyl]phenyl}quinoline

2,4-bis{4-[(3-morpholinopropyl)iminomethyl]phenyl}quinoline

Conditions
ConditionsYield
In ethanol for 5h; Reflux;98%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

2-ethoxycarbonyl-3-(p-methoxyphenylamino)quinoxaline

2-ethoxycarbonyl-3-(p-methoxyphenylamino)quinoxaline

3-((4-methoxyphenyl)amino)-N-(3-morpholinopropyl)quinoxaline-2-carboxamide

3-((4-methoxyphenyl)amino)-N-(3-morpholinopropyl)quinoxaline-2-carboxamide

Conditions
ConditionsYield
In ethanol at 80℃;98%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

pyridine-4-carbaldehyde
872-85-5

pyridine-4-carbaldehyde

(3-Morpholin-4-yl-propyl)-[1-pyridin-4-yl-meth-(E)-ylidene]-amine

(3-Morpholin-4-yl-propyl)-[1-pyridin-4-yl-meth-(E)-ylidene]-amine

Conditions
ConditionsYield
With magnesium sulfate In toluene for 18h;97%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

pyridine-4-carbaldehyde
872-85-5

pyridine-4-carbaldehyde

pyridine-4-carboxaldehyde [4-morpholinylprop-3-yl]imine
165806-86-0

pyridine-4-carboxaldehyde [4-morpholinylprop-3-yl]imine

Conditions
ConditionsYield
With magnesium sulfate In toluene for 18h;97%
With magnesium sulfate In toluene for 18h;97%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

1-<(carbonylazido)-methyl>-4-phenyl-1H-1,2,3-triazole
221461-77-4

1-<(carbonylazido)-methyl>-4-phenyl-1H-1,2,3-triazole

N-(3-morpholin-4-yl-propyl)-2-(4-phenyl-[1,2,3]triazol-1-yl)-acetamide

N-(3-morpholin-4-yl-propyl)-2-(4-phenyl-[1,2,3]triazol-1-yl)-acetamide

Conditions
ConditionsYield
In benzene for 6h; Heating;97%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

3-chloro-6-ethoxy-1,2,4-benzotriazine 1-oxide
863973-47-1

3-chloro-6-ethoxy-1,2,4-benzotriazine 1-oxide

6-ethoxy-N-[3-(4-morpholinyl)propyl]-1,2,4-benzotriazin-3-amine 1-oxide

6-ethoxy-N-[3-(4-morpholinyl)propyl]-1,2,4-benzotriazin-3-amine 1-oxide

Conditions
ConditionsYield
In 1,2-dimethoxyethane for 8h; Heating;97%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

4-propoxy-3-(5-methyl-4-oxo-7-propyl-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl)-benzenelsulfonic acid chloride
224789-27-9

4-propoxy-3-(5-methyl-4-oxo-7-propyl-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl)-benzenelsulfonic acid chloride

3-(5-methyl-4-oxo-7-propyl-3,4-dihydro-imidazo[5,1-f][1,2,4]triazin-2-yl)-N-(3-morpholin-4-yl-propyl)-4-propoxy-benzenesulfonamide

3-(5-methyl-4-oxo-7-propyl-3,4-dihydro-imidazo[5,1-f][1,2,4]triazin-2-yl)-N-(3-morpholin-4-yl-propyl)-4-propoxy-benzenesulfonamide

Conditions
ConditionsYield
97%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

2,4-dichloro-5-iodopyrimidine
13544-44-0

2,4-dichloro-5-iodopyrimidine

(2-chloro-5-iodopyrimidine-4-yl)-(3-morpholin-4-yl-propyl)-amine

(2-chloro-5-iodopyrimidine-4-yl)-(3-morpholin-4-yl-propyl)-amine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In acetonitrile at -35 - 20℃; for 72h;97%
With N-ethyl-N,N-diisopropylamine In acetonitrile at -35 - 20℃; for 73h;97%
With N-ethyl-N,N-diisopropylamine In acetonitrile at -35 - 20℃; for 73h;97%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

3-chloroindeno[1,2-c]isochromene-5,11-dione

3-chloroindeno[1,2-c]isochromene-5,11-dione

3-chloro-5,6-dihydro-6-(3-morpholinopropyl)-5,11-dioxo-11H-indeno[1,2-c]isoquinoline

3-chloro-5,6-dihydro-6-(3-morpholinopropyl)-5,11-dioxo-11H-indeno[1,2-c]isoquinoline

Conditions
ConditionsYield
In chloroform for 22h; Reflux;97%
4-(3-Aminopropyl)morpholine
123-00-2

4-(3-Aminopropyl)morpholine

(2R,4E)-10-acetyl-11,13-dihydroxy-2,12-dimethyl-4-(1-{[2-(morpholin-4-yl)propyl]amino}ethylidene)-8-oxatricyclo[7.4.0.02,7]trideca-1(9),6,10,12-tetraene-3,5-dione

(2R,4E)-10-acetyl-11,13-dihydroxy-2,12-dimethyl-4-(1-{[2-(morpholin-4-yl)propyl]amino}ethylidene)-8-oxatricyclo[7.4.0.02,7]trideca-1(9),6,10,12-tetraene-3,5-dione

Conditions
ConditionsYield
In ethanol for 3h; Reflux;97%

123-00-2Relevant articles and documents

New asymmetrical morpholinium- and 1,1-dioxidothiomorpholinium-based dicationic ionic liquid: structure, thermophysical and electrochemical properties of propylene carbonate solutions

Arkhipova, Ekaterina A.,Ivanov, Anton S.,Levin, Mikhail M.,Maslakov, Konstantin I.,Kupreenko, Stepan Yu.,Lyssenko, Konstantin A.,Savilov, Serguei V.

, (2021/08/09)

A new asymmetrical 1,1-dioxidothiomorpholinium- and morpholinium-based dicationic ionic liquid (4-ethyl-4-[3-(4-ethyl-1,1-dioxidothiomorpholin-4-ium-4-yl)propyl]morpholin-4-ium tetrafluoroborate (EtDTMC3EtM·2BF4)) was synthesized in four stages and characterized by 1H, 13C, 1H,1H–COSY NMR, single X-ray diffraction, XPS spectroscopy and simultaneous thermal analysis. Electrical conductivities of several EtDTMC3EtM·2BF4 solutions in propylene carbonate (PC) were measured in the 298 – 368 K temperature range and analyzed using the Arrhenius, Litovitz, and Vogel–Fulcher–Tammann (VFT) equations.

Highly Selective Butyrylcholinesterase Inhibitors with Tunable Duration of Action by Chemical Modification of Transferable Carbamate Units Exhibit Pronounced Neuroprotective Effect in an Alzheimer's Disease Mouse Model

Hoffmann, Matthias,Stiller, Carina,Endres, Erik,Scheiner, Matthias,Gunesch, Sandra,Sotriffer, Christoph,Maurice, Tangui,Decker, Michael

, p. 9116 - 9140 (2019/11/03)

In this study, the carbamate structure of pseudo-irreversible butyrylcholinesterase (BChE) inhibitors was optimized with regard to a longer binding to the enzyme. A set of compounds bearing different heterocycles (e.g., morpholine, tetrahydroisoquinoline, benzimidazole, piperidine) and alkylene spacers (2 to 10 methylene groups between carbamate and heterocycle) in the carbamate residue was synthesized and characterized in vitro for their binding affinity, binding kinetics, and carbamate hydrolysis. These novel BChE inhibitors are highly selective for hBChE over human acetycholinesterase (hAChE), yielding short-, medium-, and long-acting nanomolar hBChE inhibitors (with a half-life of the carbamoylated enzyme ranging from 1 to 28 h). The inhibitors show neuroprotective properties in a murine hippocampal cell line and a pharmacological mouse model of Alzheimer's disease (AD), suggesting a significant benefit of BChE inhibition for a disease-modifying treatment of AD.

Colloid and nanosized catalysts in organic synthesis: XII. Hydrogenation of carbonitriles catalyzed by nickel nanoparticles

Mokhov,Popov,Shcherbakova

, p. 273 - 280 (2016/04/20)

Hydrogenation of carbonitriles catalyzed by nickel nanoparticles in isopropanol proceeds under atmospheric pressure of hydrogen within 6-15 h to yield mainly secondary amines. Hydrogenation of α-aminonitriles results in reductive decyanation. β-Aminonitriles undergo hydrogenolysis at the nitrogen-carbon bond.

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