Assay
97%
mp
62-65 °C (lit.)
SMILES string
Sc1cc(Cl)cc(Cl)c1
InChI
1S/C6H4Cl2S/c7-4-1-5(8)3-6(9)2-4/h1-3,9H
InChI key
WRXIPCQPHZMXOO-UHFFFAOYSA-N
General description
3,5-Dichlorobenzenethiol (3,5-dichlorothiophenol) is a halogenated aromatic thiol.
Application
3,5-Dichlorobenzenethiol may be used to synthesize hyperbranched poly(phenylene sulfide) [HPPS] and bis-(3,5-dichlorophenyl) sulfide.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Low-polydispersity Hyperbranched Polyphenylene Sulfide as a Protectant for Palladium Nanocomposites.
Chemistry Letters (Jpn), 44(4), 500-502 (2015)
Semimetallic transport in nanocomposites derived from grafting of linear and hyperbranched poly (phenylene sulfide) s onto the surface of functionalized multi-walled carbon nanotubes.
Macromolecules, 41(20), 7423-7432 (2008)
Synthesis of dendritic oligo (aryl sulfone) s as supports for synthesis.
Tetrahedron, 61(52), 12314-12322 (2005)
Scientific reports, 5, 10144-10144 (2015-05-29)
Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection, and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding, and optical encoding have been
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