N,N-Diethyl-3-phenyl-3-(phenylthio)-1-propylamine oxalate

Base Information

Chemical Name:N,N-Diethyl-3-phenyl-3-(phenylthio)-1-propylamine oxalate
CAS No.:99507-50-3
Molecular Formula:C₂H₂O₄*C₁₉H₂₅NS
Molecular Weight:389.516
Hs Code.:
DSSTox Substance ID:DTXSID70912666

Synonyms:N,N-Diethyl-3-phenyl-3-(phenylthio)-1-propylamine oxalate;1-Propylamine, N,N-diethyl-3-phenyl-3-(phenylthio)-, oxalate;Benzenepropanamine, N,N-diethyl-gamma-(phenylthio)-, ethanedioate (1:1);99507-50-3;C19H25NS.C2H2O4;DTXSID70912666;C19-H25-N-S.C2-H2-O4;LS-125626;Oxalic acid--N,N-diethyl-3-phenyl-3-(phenylsulfanyl)propan-1-amine (1/1)

Suppliers and Price of N,N-Diethyl-3-phenyl-3-(phenylthio)-1-propylamine oxalate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of N,N-Diethyl-3-phenyl-3-(phenylthio)-1-propylamine oxalate

Chemical Property:

Vapor Pressure:5.86E-07mmHg at 25°C
Boiling Point:410.8°Cat760mmHg
Flash Point:202.2°C
Density:g/cm³
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:9
Exact Mass:389.16607952
Heavy Atom Count:27
Complexity:324

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CC)CCC(C1=CC=CC=C1)SC2=CC=CC=C2.C(=O)(C(=O)O)O

Technology Process of N,N-Diethyl-3-phenyl-3-(phenylthio)-1-propylamine oxalate

There total 5 articles about N,N-Diethyl-3-phenyl-3-(phenylthio)-1-propylamine oxalate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 140-10-3
(E)-3-phenylacrylic acid

: 99507-50-3
Diethyl-(3-phenyl-3-phenylsulfanyl-propyl)-amine; compound with oxalic acid

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / 6 h / 100 °C

2: thionyl chloride / benzene / 1 h / Heating

3: toluene / 6 h

4: lithium aluminum hydride / diethyl ether / 4 h / Heating

With pyridine; lithium aluminium tetrahydride; thionyl chloride; In diethyl ether; toluene; benzene;

Reference yield:

: 5425-50-3
3-phenyl-3-(phenylmercapto)propanoic acid

: 99507-50-3
Diethyl-(3-phenyl-3-phenylsulfanyl-propyl)-amine; compound with oxalic acid

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / benzene / 1 h / Heating

2: toluene / 6 h

3: lithium aluminum hydride / diethyl ether / 4 h / Heating

With lithium aluminium tetrahydride; thionyl chloride; In diethyl ether; toluene; benzene;

Reference yield:

: 61955-78-0
3-Phenyl-3-phenylthiopropionylchlorid

: 99507-50-3
Diethyl-(3-phenyl-3-phenylsulfanyl-propyl)-amine; compound with oxalic acid

Guidance literature:: Multi-step reaction with 2 steps

1: toluene / 6 h

2: lithium aluminum hydride / diethyl ether / 4 h / Heating

With lithium aluminium tetrahydride; In diethyl ether; toluene;