T33200
Thiosalicylic acid
97%
Synonym(s):
2-Sulfanylbenzoic acid, 2-Mercaptobenzoic acid
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About This Item
Linear Formula:
HSC6H4CO2H
CAS Number:
Molecular Weight:
154.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-704-3
Beilstein/REAXYS Number:
508507
MDL number:
Assay:
97%
InChI key
NBOMNTLFRHMDEZ-UHFFFAOYSA-N
InChI
1S/C7H6O2S/c8-7(9)5-3-1-2-4-6(5)10/h1-4,10H,(H,8,9)
SMILES string
OC(=O)c1ccccc1S
assay
97%
Quality Level
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Application
Thiosalicylic acid can be used as:
It can also be used to prepare 2-thioxanthone-thioacetic acid bimolecular system, which is used as a photoinitiator for free radical polymerization.
- A nucleophilic trapping agent for the desulfenylation of 3-indolyl sulfides to obtain 3-unsubstituted indoles.
- A starting material to prepare 2′-mercaptoacetophenone, which is used in the synthesis of thioflavanone by reacting with lithium diisopropylamide and benzaldehyde.
- A stabilizing agent in the synthesis of metal nanoparticles.
It can also be used to prepare 2-thioxanthone-thioacetic acid bimolecular system, which is used as a photoinitiator for free radical polymerization.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis, 309-309 (1994)
Elisabet Bermudo et al.
Journal of chromatography. A, 1129(1), 129-134 (2006-07-18)
Two in-line preconcentration capillary zone electrophoresis (CZE) methods (field amplified sample injection (FASI) and stacking with sample matrix removal (LVSS)) have been evaluated for the analysis of acrylamide (AA) in foodstuffs. To allow the determination of AA by CZE, it
R Grossman et al.
NeuroImage, 20(4), 1971-1981 (2003-12-20)
Increases in peripheral type benzodiazepine receptors (PTBR) have been utilized for the detection of neuroinflammation and neurotoxicity in the brain. We have investigated the relationship between PTBR and NMDA receptor binding density in mice with closed head injury (CHI) using
Synthesis and characterization of thiosalicylic acid stabilized gold nanoparticles
Pattabi RM and Pattabi M
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 74(1), 195-199 (2009)
K D Dobson et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56(3), 557-565 (2000-05-04)
In situ infrared spectroscopy has been used to investigate the adsorption of a range of simple aromatic carboxylic acids from aqueous solution to metal oxides. Thin films of TiO2, ZrO2, Al2O3 and Ta2O5 were prepared by evaporation of aqueous sols
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