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124668-49-1

  • Product Name3-(Dimethylamino)azetidine Dihydrochloride
  • Molecular FormulaC5H12N2.2ClH
  • Molecular Weight173.084
  • Purity99%
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Product Details

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  • CasNo: 124668-49-1
  • Molecular Formula: C5H12N2.2ClH
  • Purity: 99%

High Grade 3-(Dimethylamino)azetidine Dihydrochloride 124668-49-1 Global

  • Molecular Formula:C5H12N2.2ClH
  • Molecular Weight:173.08400
  • Vapor Pressure:6.701mmHg at 25°C 
  • Boiling Point:138.528oC at 760 mmHg 
  • Flash Point:47.914oC 
  • PSA:15.27000 
  • Density:0.933g/cm3 
  • LogP:1.45260 

3-(DIMETHYLAMINO)AZETIDINE DIHYDROCHLORIDE(Cas 124668-49-1) Usage

InChI:InChI=1/C5H12N2/c1-7(2)5-3-6-4-5/h5-6H,3-4H2,1-2H3

124668-49-1 Relevant articles

CYCLIC AMINE DERIVATIVE AND PHARMACEUTICAL USE THEREOF

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Paragraph 0137-0138, (2018/04/19)

A cyclic amine derivative represented by...

2,3,4,6-TETRA-SUBSTITUTED BENZENE-1,5-DIAMINE DERIVATIVES, PREPARATION METHOD THEREFOR AND MEDICINAL USE THEREOF

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Paragraph 0293; 0294, (2017/03/21)

The present invention relates to 2,3,4,6...

2,4-DISUBSTITUTED 7H-PYRROLO[2,3-D]PYRIMIDINE DERIVATIVE, PREPARATION METHOD AND MEDICINAL USE THEREOF

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Paragraph 0145; 0147, (2017/06/19)

The present invention relates to a 2,4-d...

2 - (2, 4, 5 - SUBSTITUTED -ANILINO) PYRIMIDINE DERIVATIVES AS EGFR MODULATORS USEFUL FOR TREATING CANCER

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Page/Page column 94; 95, (2013/03/26)

The present invention relates to certain...

124668-49-1 Process route

3-(dimethylamino)-1-(diphenylmethyl)azetidine
55438-79-4

3-(dimethylamino)-1-(diphenylmethyl)azetidine

3-(dimethylamino)azetidine dihydrochloride
124668-49-1

3-(dimethylamino)azetidine dihydrochloride

Conditions
Conditions Yield
3-(dimethylamino)-1-(diphenylmethyl)azetidine; With hydrogen; palladium(II) hydroxide/carbon; In ethanol; for 18h;
With hydrogenchloride; In ethanol;
87%
3-(dimethylamino)-1-(diphenylmethyl)azetidine; With hydrogen; dimethyl amine; palladium(II) hydroxide/carbon; In ethanol; for 18h;
With hydrogenchloride; In ethanol;
87%
With hydrogenchloride; hydrogen; palladium(II) hydroxide/carbon; In ethanol; for 18h;
87%
With hydrogenchloride; hydrogen; palladium on activated charcoal; In methanol;
With hydrogenchloride; palladium dihydroxide; hydrogen; Multistep reaction; 1) Et2O, 0 deg C; 2) EtOH, 60psi, r.t.;
tert-butyl 3-(dimethylamino)azetidine-1-carboxylate
792970-55-9

tert-butyl 3-(dimethylamino)azetidine-1-carboxylate

3-(dimethylamino)azetidine dihydrochloride
124668-49-1

3-(dimethylamino)azetidine dihydrochloride

Conditions
Conditions Yield
With hydrogenchloride; In 1,4-dioxane; dichloromethane; at 20 ℃; for 3h;
82%
With hydrogenchloride; In 1,4-dioxane; at 0 - 20 ℃; for 3h;
82%

124668-49-1 Upstream products

  • 55438-79-4
    55438-79-4

    3-(dimethylamino)-1-(diphenylmethyl)azetidine

  • 792970-55-9
    792970-55-9

    tert-butyl 3-(dimethylamino)azetidine-1-carboxylate

  • 398489-26-4
    398489-26-4

    tert-butyl 3-oxoazetidine-1-carboxylate

  • 124-40-3
    124-40-3

    dimethyl amine

124668-49-1 Downstream products

  • 1421373-30-9
    1421373-30-9

    N-[4-(3-dimethylaminoazetidin-1-yl)-2-methoxy-5-nitrophenyl]-4-(1H-indol-3-yl)pyrimidin-2-amine

  • 1421372-84-0
    1421372-84-0

    5-chloro-N-[4-(3-dimethylaminoazetidin-1-yl)-2-methoxy-5-nitrophenyl]-4-(1H-indol-3-yl)pyrimidin-2-amine

  • 1421372-80-6
    1421372-80-6

    N-[4-(3-dimethylaminoazetidin-1-yl)-2-methoxy-5-nitrophenyl]-5-methyl-4-(1-methylindol-3-yl)pyrimidin-2-amine

  • 1421373-20-7
    1421373-20-7

    N-[4-(3-dimethylaminoazetidin-1-yl)-2-methoxy-5-nitrophenyl]-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine

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