{5-Chloro-2-[(thiophen-2-yl)sulfanyl]phenyl}acetic acid

Base Information

Chemical Name:{5-Chloro-2-[(thiophen-2-yl)sulfanyl]phenyl}acetic acid
CAS No.:89011-37-0
Molecular Formula:C₁₂H₉ClO₂S₂
Molecular Weight:284.787
Hs Code.:
DSSTox Substance ID:DTXSID70526429
Wikidata:Q82394862

Synonyms:89011-37-0;{5-Chloro-2-[(thiophen-2-yl)sulfanyl]phenyl}acetic acid;DTXSID70526429

Suppliers and Price of {5-Chloro-2-[(thiophen-2-yl)sulfanyl]phenyl}acetic acid

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 1 raw suppliers

Chemical Property of {5-Chloro-2-[(thiophen-2-yl)sulfanyl]phenyl}acetic acid

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:283.9732496
Heavy Atom Count:17
Complexity:275

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CSC(=C1)SC2=C(C=C(C=C2)Cl)CC(=O)O

Technology Process of {5-Chloro-2-[(thiophen-2-yl)sulfanyl]phenyl}acetic acid

There total 3 articles about {5-Chloro-2-[(thiophen-2-yl)sulfanyl]phenyl}acetic acid 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:

: 2476-37-1
2,5-dichloroacetophenone

: 89011-37-0
<5-Chloro-2-(2-thienylthio)phenyl>acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 41 percent / K₂CO₃ / Cu / 1 h / 130 - 140 °C

2: Sulphur / 2 h / Heating

3: KOH / ethanol / 2.5 h / Heating

With potassium hydroxide; potassium carbonate; sulfur; copper; In ethanol;
DOI:10.1135/cccc19832970

Reference yield:

: 89011-36-9
<5-Chloro-2-(2-thienylthio)phenyl>acetic acid thiomorpholide

: 13125-02-5
5-Chloro-2-(2-thienylthio)benzoic acid

: 89011-37-0
<5-Chloro-2-(2-thienylthio)phenyl>acetic acid

Guidance literature:: With potassium hydroxide; In ethanol; for 2.5h; Yield given; Heating;
DOI:10.1135/cccc19832970

Reference yield:

: 89011-34-7
5-Chloro-2-(2-thienylthio)acetophenone

: 89011-37-0
<5-Chloro-2-(2-thienylthio)phenyl>acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: Sulphur / 2 h / Heating

2: KOH / ethanol / 2.5 h / Heating

With potassium hydroxide; sulfur; In ethanol;
DOI:10.1135/cccc19832970