Formamide, N-[2-[3-(methylthio)phenyl]ethyl]-

Base Information

Chemical Name:Formamide, N-[2-[3-(methylthio)phenyl]ethyl]-
CAS No.:90265-79-5
Molecular Formula:C10H13NOS
Molecular Weight:195.285
Hs Code.:
DSSTox Substance ID:DTXSID30450433
Wikidata:Q82270159

Synonyms:90265-79-5;Formamide, N-[2-[3-(methylthio)phenyl]ethyl]-;N-[2-(3-Methylsulfanyl-phenyl)-ethyl]-formamide;SCHEMBL6797584;DTXSID30450433;PVHBRXMKIXEUEQ-UHFFFAOYSA-N

Suppliers and Price of Formamide, N-[2-[3-(methylthio)phenyl]ethyl]-

Supply Marketing:

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

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Chemical Property of Formamide, N-[2-[3-(methylthio)phenyl]ethyl]-

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:195.07178521
Heavy Atom Count:13
Complexity:152

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CSC1=CC=CC(=C1)CCNC=O

Technology Process of Formamide, N-[2-[3-(methylthio)phenyl]ethyl]-

There total 7 articles about Formamide, N-[2-[3-(methylthio)phenyl]ethyl]- 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: 98.0%

: 118468-20-5
2-(3-methylsulfanyl-phenyl)ethylamine

: 109-94-4
formic acid ethyl ester

: 90265-79-5
N-formyl-2-(3-methylthiophenyl)ethylamine

Guidance literature:: for 3h; Heating;

Reference yield: 78.0%

: 90265-79-5
N-formyl-2-(3-methylthiophenyl)ethylamine

Guidance literature:

Reference yield:

: 59083-33-9
(3-methylsulfanyl-phenyl)-methanol

: 90265-79-5
N-formyl-2-(3-methylthiophenyl)ethylamine

Guidance literature:: Multi-step reaction with 5 steps

1: SOCl₂ / benzene / 48 h / 20 °C

2: 22.9 g / 18-crown-6 / acetonitrile / 48 h / 20 °C

3: 33 percent / Raney nickel / methanol / 48 h / 20 °C

4: 99 percent / CF₃CO₂H / 0.17 h / 20 °C

5: Heating

With thionyl chloride; 18-crown-6 ether; nickel; trifluoroacetic acid; In methanol; acetonitrile; benzene;
DOI:10.1021/jm011116o