Propanamide, 3,3'-dithiobis[N-(2-phenylethyl)-

Base Information

Chemical Name:Propanamide, 3,3'-dithiobis[N-(2-phenylethyl)-
CAS No.:33312-15-1
Molecular Formula:C22H28N2O2S2
Molecular Weight:416.609
Hs Code.:
DSSTox Substance ID:DTXSID90469324
Nikkaji Number:J2.244.908G
Wikidata:Q82296990

Synonyms:Propanamide, 3,3'-dithiobis[N-(2-phenylethyl)-;33312-15-1;SCHEMBL9516616;DTXSID90469324

Suppliers and Price of Propanamide, 3,3'-dithiobis[N-(2-phenylethyl)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Propanamide, 3,3'-dithiobis[N-(2-phenylethyl)-

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:13
Exact Mass:416.15922049
Heavy Atom Count:28
Complexity:396

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CCNC(=O)CCSSCCC(=O)NCCC2=CC=CC=C2

Technology Process of Propanamide, 3,3'-dithiobis[N-(2-phenylethyl)-

There total 6 articles about Propanamide, 3,3'-dithiobis[N-(2-phenylethyl)- 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: 66.0%

: 102337-31-5
N-phenethyl 3-mercaptopropionamide

: 33312-15-1
3,3'-disulfanediylbis(N-phenethylpropanamide)

Guidance literature:: With sodium hydroxide; TEMPO oxoammonium ion; In acetonitrile; at 20 ℃; for 1h;
DOI:10.1021/jo050783c

Reference yield:

: thiobenzoic acid S-(2-phenethylcarbamoyl-ethyl) ester

: 33312-15-1
3,3'-disulfanediylbis(N-phenethylpropanamide)

Guidance literature:: Multi-step reaction with 2 steps

1: 1.3 g / NaOH

2: 66 percent / TEMPO oxoammonium ion; aq. NaOH / acetonitrile / 1 h / 20 °C

With sodium hydroxide; TEMPO oxoammonium ion; In acetonitrile;
DOI:10.1021/jo050783c

Reference yield:

: 70875-36-4
N-(β-phenethyl)-3-bromopropionamide

: 33312-15-1
3,3'-disulfanediylbis(N-phenethylpropanamide)

Guidance literature:: Multi-step reaction with 3 steps

1: 1.3 g / NaOH

2: 66 percent / TEMPO oxoammonium ion; aq. NaOH / acetonitrile / 1 h / 20 °C

With sodium hydroxide; TEMPO oxoammonium ion; In acetonitrile;
DOI:10.1021/jo050783c