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Merck
CN

540870

3,5-Dichlorobenzenethiol

97%

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About This Item

Linear Formula:
Cl2C6H3SH
CAS Number:
Molecular Weight:
179.07
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
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InChI

1S/C6H4Cl2S/c7-4-1-5(8)3-6(9)2-4/h1-3,9H

SMILES string

Sc1cc(Cl)cc(Cl)c1

InChI key

WRXIPCQPHZMXOO-UHFFFAOYSA-N

assay

97%

mp

62-65 °C (lit.)

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.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

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

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Low-polydispersity Hyperbranched Polyphenylene Sulfide as a Protectant for Palladium Nanocomposites.
Meng Y, et al.
Chemistry Letters (Jpn), 44(4), 500-502 (2015)
Synthesis of dendritic oligo (aryl sulfone) s as supports for synthesis.
Taylor PC, et al.
Tetrahedron, 61(52), 12314-12322 (2005)
Semimetallic transport in nanocomposites derived from grafting of linear and hyperbranched poly (phenylene sulfide) s onto the surface of functionalized multi-walled carbon nanotubes.
Jeon IY, et al.
Macromolecules, 41(20), 7423-7432 (2008)
Homan Kang et al.
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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