S-phenyl 2-chloropropanethioate

Base Information

Chemical Name:S-phenyl 2-chloropropanethioate
CAS No.:120346-68-1
Molecular Formula:C9H9ClOS
Molecular Weight:200.689
Hs Code.:
DSSTox Substance ID:DTXSID30518380
Nikkaji Number:J450.455K

Synonyms:S-phenyl 2-chloropropanethioate;120346-68-1;DTXSID30518380;2-chloro-propanethioic acid S-phenyl ester

Suppliers and Price of S-phenyl 2-chloropropanethioate

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 0 raw suppliers

Chemical Property of S-phenyl 2-chloropropanethioate

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:200.0062638
Heavy Atom Count:12
Complexity:155

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C(=O)SC1=CC=CC=C1)Cl

Technology Process of S-phenyl 2-chloropropanethioate

There total 5 articles about S-phenyl 2-chloropropanethioate 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: 99.0%

: 120346-61-4
(E)-3-methyl-2-phenylsulphonyl-2-phenylthiooxirane

: 120346-68-1
S-phenyl 2-chloro(thiopropanoate)

Guidance literature:: With lithium chloride; In acetone; for 5h; Ambient temperature;
DOI:10.1039/P19910003091

Reference yield:

: 15296-86-3
1-(phenylsulfanyl)methyl phenyl sulfone

: 120346-68-1
S-phenyl 2-chloro(thiopropanoate)

Guidance literature:: Multi-step reaction with 3 steps

2: 99 percent / lithium tert-butyl hydroperoxide / tetrahydrofuran; toluene / 0.5 h / -78 °C

3: 99 percent / lithium chloride / acetone / 5 h / Ambient temperature

With lithium tert-butyl hydroperoxide; lithium chloride; In tetrahydrofuran; acetone; toluene;
DOI:10.1039/P19910003091

Reference yield:

: 120346-57-8
(E)-1-phenylsulphonyl-1-phenylthioprop-1-ene

: 120346-68-1
S-phenyl 2-chloro(thiopropanoate)

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / lithium tert-butyl hydroperoxide / tetrahydrofuran; toluene / 0.5 h / -78 °C

2: 99 percent / lithium chloride / acetone / 5 h / Ambient temperature

With lithium tert-butyl hydroperoxide; lithium chloride; In tetrahydrofuran; acetone; toluene;
DOI:10.1039/P19910003091