1-[(2-Chloroethyl)thio]-4-fluorobenzene

Base Information

Chemical Name:1-[(2-Chloroethyl)thio]-4-fluorobenzene
CAS No.:5323-03-5
Molecular Formula:C15H9ClN2O3
Molecular Weight:0
Hs Code.:2930909090
DSSTox Substance ID:DTXSID90406976
Mol file:5323-03-5.mol

Synonyms:1-[(2-chloroethyl)thio]-4-fluorobenzene;5323-03-5;1-[(2-chloroethyl)sulfanyl]-4-fluorobenzene;1-(2-chloroethylsulfanyl)-4-fluorobenzene;(2-chloroethyl)(4-fluorophenyl)sulfane;SCHEMBL4186269;DTXSID90406976;2-(4-fluorophenylthio)ethyl chloride;AKOS008039311;CS-0225922;EN300-12524

Suppliers and Price of 1-[(2-Chloroethyl)thio]-4-fluorobenzene

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

American Custom Chemicals Corporation
1-[(2-CHLOROETHYL)THIO]-4-FLUOROBENZENE 95.00%
2.5G
$ 1227.82

American Custom Chemicals Corporation
1-[(2-CHLOROETHYL)THIO]-4-FLUOROBENZENE 95.00%
1G
$ 453.60

AK Scientific
1-[(2-Chloroethyl)thio]-4-fluorobenzene
10g
$ 1836.00

AK Scientific
1-[(2-Chloroethyl)thio]-4-fluorobenzene
2.5g
$ 892.00

Total 5 raw suppliers

Chemical Property of 1-[(2-Chloroethyl)thio]-4-fluorobenzene

Chemical Property:

Vapor Pressure:0.04mmHg at 25°C
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：25.30000
Density:1.53g/cm³
LogP:3.15660
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:190.0019273
Heavy Atom Count:11
Complexity:102

Purity/Quality:

99% ^*data from raw suppliers

1-[(2-CHLOROETHYL)THIO]-4-FLUOROBENZENE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1F)SCCCl

Technology Process of 1-[(2-Chloroethyl)thio]-4-fluorobenzene

There total 5 articles about 1-[(2-Chloroethyl)thio]-4-fluorobenzene 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%

: 371-42-6
4-Fluorothiophenol

: 107-06-2,52399-93-6
1,2-dichloro-ethane

: 5323-03-5
(2-chloroethyl)(4-fluorophenyl)sulfane

Guidance literature:

Reference yield:

: 5322-63-4
2-[(4-fluorophenyl)thio]ethanol

: 5323-03-5
(2-chloroethyl)(4-fluorophenyl)sulfane

Guidance literature:: With pyridine; thionyl chloride;
DOI:10.1021/jm00297a033

Reference yield:

: 371-42-6
4-Fluorothiophenol

: 5323-03-5
(2-chloroethyl)(4-fluorophenyl)sulfane

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH

2: SOCl₂, Py

With pyridine; sodium hydroxide; thionyl chloride;
DOI:10.1021/jm00297a033