ChemAbout
© 2026 ChemAbout
Insights|Privacy Policy|Terms of Service|[email protected]
Home/Compounds/Other/2-[(4-Chlorophenyl)thio]benzeneacetic acid
C14H11ClO2S
278.8 g/mol
Other

2-(2-((4-Chlorophenyl)thio)phenyl)acetic acid

CAS13459-62-6
Category
Other
Compound Class
n.a
Primary Use
research compound

This compound is a chlorinated aromatic carboxylic acid containing a sulfur-linked biphenyl structure and a single carboxylic acid group. It is a relatively nonpolar molecule with moderate lipophilicity and is used as a research reagent.

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

Sourcing or supplying this compound?

List your inventory or post a purchase request

CAS 13459-62-6

List This Product
Sign in to publish supply information
Request This Product
Submit a request without registering

Related Compounds

ReferenceSame Category

Tetrakis[(pivaloyloxy)methyl] methylenediphosphonate

CAS134606-34-1

research compound

ReferenceSame Category

Acetyl 2-[(2-Formamide-1,6-dihydro-6-chloro-9H-purin-9yl)methoxy]ethyl Ester

CAS1346598-89-7

Research compound for pharmaceutical impurity analysis

ReferenceSame Category

5-bromopyridin-2(1H)-one

CAS13466-38-1

Laboratory reagent

ReferenceSame Category

3,3'-(((1,2-phenylenebis(oxy))bis(ethane-2,1-diyl))bis(azanediyl))bis(1-((9H-carbazol-4-yl)oxy)propan-2-ol)

CAS1346602-98-9

compound for research

Referencesame scaffold

I+/--Oxo-2-(phenylthio)benzenepropanoic acid

CAS36943-41-6

research compound

Referencesame scaffold

4,4'-thiodianiline

CAS139-65-1

Dye intermediate

Referencesame scaffold

Diphenyl sulfide

CAS139-66-2

organosulfur compound intermediate

Referencesame scaffold

2,2'-Thiobis(4-tert-octylphenolato)-n-butylamine nickel(II)

CAS14516-71-3

UV absorber for plastics

Identifiers
IUPAC Name

2-[2-(4-chlorophenyl)sulfanylphenyl]acetic acid

InChIKey

WZICWIASCZNZHO-UHFFFAOYSA-N

SMILES

C1=CC=C(C(=C1)CC(=O)O)SC2=CC=C(C=C2)Cl

Synonyms (5)

—