What is the 4-(2-Aminoethyl)morpholine?

4-(2-Aminoethyl)morpholine is clear colorless to pale yellow liq. after melting, while it's Molecular Formula is C6H14N2O. clear colorless to pale yellow liq. after melting 4-(2-Aminoethyl)morpholine is widely used in biomedical applications as this moiety serves as an important lysosome-targeting group. Some of its applications include:Synthesis of the lysosome-targetable fluorescent probe for hydrogen sulfide imaging in living cells.Synthesis of 1,8-naphthalimide conjugated Troger's bases as deoxyribonucleic acid (DNA) targeting fluorescent probe.Synthesis of intramolecular charge transfer-photoinduced electron transfer-fluorescence resonance energy transfer (ICT-PET-FRET) fluorescent probe for monitoring pH changes in living cells.It is also used as a precursor to synthesize a variety of antimicrobial agents.

What is the CAS number for 4-(2-Aminoethyl)morpholine?

The CAS number of 4-(2-Aminoethyl)morpholine is 2038-03-1.

What is 4-(2-Aminoethyl)morpholine (2038-03-1) used for?

4-(2-Aminoethyl)morpholine is a colorless to pale yellow liquid that serves as a versatile ligand and building block in various chemical and biomedical applications due to its unique chemical structure and properties.InChI:InChI=1/C6H14N2O/c7-1-2-8-3-5-9-6-4-8/h1-7H2/p+2

What is the 4-(2-Aminoethyl)morpholine?

4-(2-Aminoethyl)morpholine is clear colorless to pale yellow liq. after melting, while it's Molecular Formula is C6H14N2O. clear colorless to pale yellow liq. after melting 4-(2-Aminoethyl)morpholine is widely used in biomedical applications as this moiety serves as an important lysosome-targeting group. Some of its applications include:Synthesis of the lysosome-targetable fluorescent probe for hydrogen sulfide imaging in living cells.Synthesis of 1,8-naphthalimide conjugated Troger′s bases as deoxyribonucleic acid (DNA) targeting fluorescent probe.Synthesis of intramolecular charge transfer-photoinduced electron transfer-fluorescence resonance energy transfer (ICT-PET-FRET) fluorescent probe for monitoring pH changes in living cells.It is also used as a precursor to synthesize a variety of antimicrobial agents.

What is the CAS number for 4-(2-Aminoethyl)morpholine?

The CAS number of 4-(2-Aminoethyl)morpholine is 2038-03-1.

What is 4-(2-Aminoethyl)morpholine (2038-03-1) used for?

4-(2-Aminoethyl)morpholine is a colorless to pale yellow liquid that serves as a versatile ligand and building block in various chemical and biomedical applications due to its unique chemical structure and properties.InChI:InChI=1/C6H14N2O/c7-1-2-8-3-5-9-6-4-8/h1-7H2/p+2

4-(2-Aminoethyl)morpholine

Quality Factory Sells Top Purity 99% 4-(2-Aminoethyl)morpholine 2038-03-1 with Safe Delivery

Molecular Formula: C6H14N2O
Molecular Weight: 130.19
Appearance/Colour: clear colorless to pale yellow liq. after melting
Vapor Pressure: 0.289mmHg at 25°C
Melting Point: 24 °C
Refractive Index: n20/D 1.476(lit.)
Boiling Point: 202.6 °C at 760 mmHg
PKA: pK1: 4.06(+2);pK2: 9.15(+1) (25°C)
Flash Point: 76.3 °C
PSA： 38.49000
Density: 1.002 g/cm³
LogP: -0.08450

4-(2-Aminoethyl)morpholine(Cas 2038-03-1) Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 34, p. 1805, 1991 DOI: 10.1021/jm00110a008

InChI:InChI=1/C6H14N2O/c7-1-2-8-3-5-9-6-4-8/h1-7H2/p+2

2038-03-1 Relevant articles

SYNTHESIS, STRUCTURE, AND ACTION OF SOME GOSSYPOL DERIVATIVES ON THE PEROXIDATION OF THE LIPIDS OF BIOSUBSTRATES

Dalimov, D. N.,Mukhamedzhanova, E. N.,Shneivais, V. B.,Biktimirov, L.,Ismailov, A. I.,Kamaev, F. G.

, p. 603 - 607 (1989)

The synthesis has been effected of new g...

Preparation method of N-(2-aminoethyl) morpholine

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Paragraph 0062; 0069-0072; 0073; 0080-0083, (2021/04/21)

The invention provides a preparation met...

COMPOUND INHIBITING BUTYRYLCHOLINESTERASE

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Page/Page column 9, (2020/07/31)

The invention concerns a compound accord...

New pyrido[3,4-g]quinazoline derivatives as CLK1 and DYRK1A inhibitors: synthesis, biological evaluation and binding mode analysis

Tazarki, Helmi,Zeinyeh, Wael,Esvan, Yannick J.,Knapp, Stefan,Chatterjee, Deep,Schr?der, Martin,Joerger, Andreas C.,Khiari, Jameleddine,Josselin, Béatrice,Baratte, Blandine,Bach, Stéphane,Ruchaud, Sandrine,Anizon, Fabrice,Giraud, Francis,Moreau, Pascale

, p. 304 - 317 (2019/02/07)

Cdc2-like kinase 1 (CLK1) and dual speci...

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 o...

2038-03-1 Process route

: 5807-02-3
4-morpholinoacetonitrile

: 2038-03-1
4-(2-AMINOETHYL)MORPHOLINE

Conditions

Conditions	Yield
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 3.33333h;	72%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 3h; Reflux;	72%
With lithium aluminium tetrahydride; In tetrahydrofuran; for 3h; Reflux;	72%
With ethanol; sodium; toluene;
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 3h; Reflux;

: 6820-90-2
2-(2-morpholin-4-ylethyl)-1H-isoindole-1,3(2H)-dione

: 2038-03-1
4-(2-AMINOETHYL)MORPHOLINE

Conditions

Conditions	Yield
With hydrazine hydrate; In ethanol; for 24h; Reflux;	95%
With hydrazine hydrate; In ethanol; at 20 ℃; Reflux;	95%
With hydrogenchloride;
With hydrazine hydrate; In ethanol; Reflux;
With hydrazine hydrate; In ethanol; for 18h; Reflux;