3-(Phenylsulfanyl)propanoyl chloride

Base Information

Chemical Name:3-(Phenylsulfanyl)propanoyl chloride
CAS No.:51849-21-9
Molecular Formula:C9H9ClOS
Molecular Weight:200.689
Hs Code.:
DSSTox Substance ID:DTXSID50507918
Nikkaji Number:J875.921I
Wikidata:Q82364495
Mol file:51849-21-9.mol

Synonyms:51849-21-9;3-(phenylsulfanyl)propanoyl chloride;3-(phenylthio)propanoyl chloride;3-phenylsulfanylpropanoyl chloride;3-(phenylthio)propanoylchloride;b-(Phenylthio)propionyl chloride;DTXSID50507918;AKOS015957359;CS-0270229;EN300-239013;F2158-0702

Suppliers and Price of 3-(Phenylsulfanyl)propanoyl chloride

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
Packaging
price

Total 4 raw suppliers

Chemical Property of 3-(Phenylsulfanyl)propanoyl chloride

Chemical Property:

PSA：42.37000
LogP:2.93420
XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:200.0062638
Heavy Atom Count:12
Complexity:144

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)SCCC(=O)Cl

Technology Process of 3-(Phenylsulfanyl)propanoyl chloride

There total 5 articles about 3-(Phenylsulfanyl)propanoyl chloride 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%

: 5219-65-8
acide phenylthio-3 propanoique

: 51849-21-9
β-(phenylthio)propionyl chloride

Guidance literature:: With thionyl chloride; In dichloromethane; 1.) 0 deg C, 1 h, 2.) r.t., overnight;
DOI:10.1021/jo00090a036

Reference yield:

: 108-98-5
thiophenol

: 51849-21-9
β-(phenylthio)propionyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / Et₃N / tetrahydrofuran / 1.) 0 deg C, 1 h, 2.) r.t., overnight

2: 98 percent / SOCl₂ / CH₂Cl₂ / 1.) 0 deg C, 1 h, 2.) r.t., overnight

With thionyl chloride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo00090a036

Reference yield:

: 108-98-5
thiophenol

: 51849-21-9
β-(phenylthio)propionyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / KOH / ethanol / 2 h / Heating

2: oxalyl chloride / 2 h / 20 °C

With potassium hydroxide; oxalyl dichloride; In ethanol;
DOI:10.1248/cpb.48.1854