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Chemical Structure| 19475-28-6 Chemical Structure| 19475-28-6

Structure of 19475-28-6

Chemical Structure| 19475-28-6

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Product Details of [ 19475-28-6 ]

CAS No. :19475-28-6
Formula : C8H20N2
M.W : 144.26
SMILES Code : CCCNCCCN(C)C
MDL No. :MFCD11146411
InChI Key :LVCAUABGOWBVQM-UHFFFAOYSA-N
Pubchem ID :14089424

Safety of [ 19475-28-6 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H314
Precautionary Statements:P210-P233-P240-P241-P242-P243-P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P370+P378-P403+P235-P405-P501
Class:8(3)
UN#:2734
Packing Group:

Application In Synthesis of [ 19475-28-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 19475-28-6 ]

[ 19475-28-6 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 50-00-0 ]
  • [ 19475-28-6 ]
  • [ 143-33-9 ]
  • N,N-Dimethyl-N'-propyl-N'-cyanmethyl-trimethylendiamin [ No CAS ]
  • 3
  • [ 19475-28-6 ]
  • [ 107-13-1 ]
  • N,N-Dimethyl-N'-propyl-N'-β-cyanethyl-trimethylendiamin [ No CAS ]
  • 4
  • [ 19475-28-6 ]
  • 2-chloro-4-(3-methyl-3<i>H</i>-benzothiazol-2-ylidenemethyl)-1-phenyl-quinolinium; iodide [ No CAS ]
  • N',N'-dimethyl-N-[4-[(E)-(3-methyl-1,3-benzothiazol-2-ylidene)methyl]-1-phenylquinolin-1-ium-2-yl]-N-propylpropane-1,3-diamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 18 N,N-Dimethyl-N'-propyl-1,3-propanediamine To a solution of 3-dimethylaminopropane (2.0 g, 20 mmole) in tetrahydrofuran was added propionyl chloride (1.8 mL, 20 mmole) dropwise. The reaction mixture was stirred at room temperature overnight. To the reaction mixture was added a solution of 1M lithium aluminumhydride in tetrahydrofuran (19.5 mL). The reaction mixture was refluxed for 6 hours then cooled to room temperature. The reaction mixture was quenched slowly and sequentially with water (10 drops), 15% aqueous sodium hydroxide (10 drops) and water (30 drops). The precipitate was filtered and the solvent removed under reduced pressure. Excess water was removed by azetroping with benzene. The crude material was carried on to the next step.
  • 8
  • [ 24424-99-5 ]
  • [ 19475-28-6 ]
  • N-boc-propyl-(3-dimethylaminopropyl)amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; N-Boc-propyl-(3-N',N'-dimethylaminopropyl)amine. Di-t-butyl-dicarbonate (2.4 g, 11 mmoles) was dissolved in 35 mL of dichloromethane and the solution was stirred in ice/water bath, followed by adding drop-wise of a solution of <strong>[19475-28-6]Propyl-(3-N',N'-dimethylaminopropyl)amine</strong> (1.44 g, 10 mmoles) and triethylamine (6.3 mL, 50 mmoles) in 15 mL of dichloromethane. After addition, the solution was stirred at room temperature overnight. Then, the solution was washed twice with water, the solvent was removed under reduced pressure, and 1.7 g of colorless oil was obtained. MS+ 245.1; 1H-NMR (CD2Cl2) δ ppm 3.22-3.08 (m, 4H), 2.25-2.15 (m, 8H), 1.71-1.59 (m, 2H), 1.59-1.45 (m, 2H), 1.44 (s, 9H), 0.90-0.82 (t, 3H).
1.7 g With triethylamine; In dichloromethane; at 20.0℃; Di-t-butyl-dicarbonate (2.4 g, 11 mmoles) was dissolved in 35 mE of dichloromethane and the solution was stirred inice/water bath, followed by adding drop-wise of a solution ofPropyl-(3-N’,N’-dimethylaminopropyl)amine (1.44 g, 10mmoles) and triethylamine (6.3 mE, 50 mmoles) in 15 mE of dichloromethane. After addition, the solution was stirred at room temperature overnight. Then, the solution was washed twice with water, the solvent was removed under reducedoressure and 1.7 g of colorless oil was obtained. MS 245.11RNMR (CD2C12) ö ppm 3.22-3.08 (m, 4R), 2.25-2.15 (m,8R), 1.71-1.59 (m, 2R), 1.59-1.45 (m, 2R), 1.44 (s, 9R),0.90-0.82 (t, 3R).
  • 9
  • [ 19475-28-6 ]
  • 3-(propylamino)propyl-N',N',N'-trimethylammonium iodide [ No CAS ]
  • 10
  • [ 19475-28-6 ]
  • 4-((5,6-dihydrothiazolo[5,4,3-ij]quinolin-2(4H)-ylidene)methyl)-7-methoxy-1-methyl-2-(propyl(3-(trimethylammonio)propyl)amino)quinolinium [ No CAS ]
  • 11
  • [ 19475-28-6 ]
  • 4-((5,6-dihydrothiazolo[5,4,3-ij]quinolin-2(4H)-ylidene)methyl)-7-methoxy-1-phenyl-2-(propyl(3-(trimethylammonio)propyl)amino)quinolinium [ No CAS ]
  • 12
  • [ 24424-99-5 ]
  • [ 19475-28-6 ]
  • 3-(N-boc-propylamino)propyl-N',N',N'-trimethylammonium iodide [ No CAS ]
 

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