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7144-05-0

4-(Aminomethyl)piperidine

4-(Aminomethyl)piperidine

Another Name:
CasNo.: 7144-05-0
MF: C6H14N2
MW: 114.191
Storage:
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ch_Name: 4-(Aminomethyl)piperidine
English name: 4-(Aminomethyl)piperidine
CasNo.: 7144-05-0
MF: C6H14N2
MW: 114.191

Factory Supply industrial standard 4-(Aminomethyl)piperidine 7144-05-0 In Stock

  • Molecular Formula:C6H14N2
  • Molecular Weight:114.191
  • Appearance/Colour:clear colorless to slightly yellow liquid 
  • Vapor Pressure:0.331mmHg at 25°C 
  • Melting Point:25 °C(lit.) 
  • Refractive Index:n20/D 1.49(lit.)  
  • Boiling Point:200 °C at 760 mmHg 
  • PKA:10.53±0.10(Predicted) 
  • Flash Point:78.9 °C 
  • PSA:38.05000 
  • Density:0.897 g/cm3 
  • LogP:0.97380 

4-(Aminomethyl)piperidine(Cas 7144-05-0) Usage

General Description

This product has been enhanced for energy efficiency.

InChI:InChI=1/C6H14N2/c7-5-6-1-3-8-4-2-6/h6,8H,1-5,7H2/p+2

7144-05-0 Relevant articles

Spectrophotometric and thermal studies on the charge - Transfer complexes of 4-(aminomethyl) piperidine as donor with σ- And π-electron acceptors

Mostafa, Adel,El-Ghossein, Nada,Alqaradawi, Siham Y.

, p. 1012 - 1019 (2014)

The spectroscopic characteristics of the...

Corresponding amine nitrile and method of manufacturing thereof

-

Paragraph 0240, (2017/10/22)

The invention relates to a manufacturing...

Electrophilic Zinc Homoenolates: Synthesis of Cyclopropylamines from Cyclopropanols and Amines

Mills, L. Reginald,Barrera Arbelaez, Luis Miguel,Rousseaux, Sophie A. L.

supporting information, p. 11357 - 11360 (2017/08/30)

Metal homoenolates, produced via C-C bon...

Analogs of biologically active, naturally occurring polyamines, pharmaceutical compositions and methods of treatment

-

, (2008/06/13)

Polyamines having the formula: 1or a sa...

7144-05-0 Process route

4-cyanopiperidine
4395-98-6

4-cyanopiperidine

4-Aminomethylpiperidine
7144-05-0

4-Aminomethylpiperidine

Conditions
Conditions Yield
With hydrogen; In ethanol; at 88 ℃; for 1h; under 45004.5 Torr;
92%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 16h; Reflux; Inert atmosphere;
2-mesitylenesulphonyl chloride
773-64-8

2-mesitylenesulphonyl chloride

1,4-diaminobutane
110-60-1

1,4-diaminobutane

4-Aminomethylpiperidine
7144-05-0

4-Aminomethylpiperidine

N,N'-bis(2,4,6-trimethylbenzenesulfonyl)-1,4-butanediamine
161452-28-4

N,N'-bis(2,4,6-trimethylbenzenesulfonyl)-1,4-butanediamine

Conditions
Conditions Yield
With hydrogenchloride; In sodium hydroxide; dichloromethane;
50.46 g (90%)
With hydrogenchloride; In sodium hydroxide; dichloromethane;
50.46 g (90%)
With hydrogenchloride; In sodium hydroxide; dichloromethane;
50.46 g (90%)

7144-05-0 Upstream products

  • 132431-14-2
    132431-14-2

    4-(Benzyloxycarbonylamino-methyl)-piperidine-1-carboxylic acid benzyl ester

  • 773-64-8
    773-64-8

    2-mesitylenesulphonyl chloride

  • 110-60-1
    110-60-1

    1,4-diaminobutane

  • 4395-98-6
    4395-98-6

    4-cyanopiperidine

7144-05-0 Downstream products

  • 144222-22-0
    144222-22-0

    tert-butyl 4-(aminomethyl)piperidine-1-carboxylate

  • 65017-57-4
    65017-57-4

    1-(1-butyl-4-piperidinyl)methanamine

  • 258345-24-3
    258345-24-3

    (1-iso-butyl-4-piperidyl)methylamine

  • 170353-28-3
    170353-28-3

    (1-(pyridin-2-yl)piperidin-4-yl)methanamine

No data available
No data available
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