549223
3,4-Difluorothiophenol
96%
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About This Item
Linear Formula:
F2C6H3SH
CAS Number:
Molecular Weight:
146.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
3,4-Difluorothiophenol, 96%
InChI
1S/C6H4F2S/c7-5-2-1-4(9)3-6(5)8/h1-3,9H
SMILES string
Fc1ccc(S)cc1F
InChI key
BGVRHDQMTMPAEZ-UHFFFAOYSA-N
assay
96%
refractive index
n20/D 1.528 (lit.)
bp
169-170 °C (lit.)
density
1.323 g/mL at 25 °C (lit.)
functional group
fluoro
Quality Level
Application
3,4-Difluorothiophenol may be used:
- To prepare a novel 3,4-difluorophenylthiomethyl group containing phthalazine derivative, which shows high cytotoxic activity.
- To prepare a fluorothiophenyl modified poly(vinyl chloride) membrane with improved gas permeability efficiency.
- As a ligand to synthesize noble metal quantum clusters (QCs).
- To prepare ethyl 5-(aminosulfonyl)-2-[(3,4-difluorophenyl)thio]nicotinate, an intermediate for preparing potent thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV.
General description
3,4-Difluorothiophenol is a halo-substituted thiol derivative.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
120.0 °F - closed cup
flash_point_c
48.9 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Gas transport in fluorothiophenyl modified PVC membranes.
Bierbrauer K, et al.
Journal of Membrane Science, 362(1), 164-171 (2010)
Synthesis and in vitro cytotoxicity of novel 1, 4-disubstituted phthalazines.
Zhai X, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 19(1), 29-32 (2008)
Noble metal clusters: applications in energy, environment, and biology.
Mathew A and Pradeep T.
Particle & Particle Systems Characterization, 31(10), 1017-1053 (2013)
Thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV: structure-based drug design, synthesis, and biological evaluation.
Vernier W, et al.
Bioorganic & Medicinal Chemistry, 18(9), 3307-3319 (2010)
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