347558
4-Oxo-2-thioxo-3-thiazolidinylacetic acid
≥99%
Synonym(s):
Rhodanine-3-acetic acid
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About This Item
Empirical Formula (Hill Notation):
C5H5NO3S2
CAS Number:
Molecular Weight:
191.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
227-220-1
Beilstein/REAXYS Number:
149513
MDL number:
Assay:
≥99%
Form:
solid
Product Name
4-Oxo-2-thioxo-3-thiazolidinylacetic acid, ≥99%
InChI key
JGRMXPSUZIYDRR-UHFFFAOYSA-N
InChI
1S/C5H5NO3S2/c7-3-2-11-5(10)6(3)1-4(8)9/h1-2H2,(H,8,9)
SMILES string
OC(=O)CN1C(=O)CSC1=S
assay
≥99%
form
solid
mp
145-148 °C (lit.)
solubility
methanol: soluble 25 mg/mL, clear, yellow
functional group
carboxylic acid
thioether
Quality Level
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Application
4-Oxo-2-thioxo-3-thiazolidinylacetic acid was employed as sample to investigate the uncertainty in organic elemental analysis of C, H, N and S.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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R Companyó et al.
Analytical and bioanalytical chemistry, 392(7-8), 1497-1505 (2008-10-15)
We evaluate the uncertainty in organic elemental analysis of C, H, N, and S. We use data from six proficiency tests (PTs), in which some 35 Spanish laboratories participated. The uncertainty of the technique is estimated from the relative within-laboratory
Zhen-Hua Chen et al.
European journal of medicinal chemistry, 45(12), 5739-5743 (2010-10-05)
With an intention to synergize the anti-bacterial activity of chalcones and rhodanine-3-acetic acid, several hybrid compounds possessing chalcone and rhodanine-3-acetic acid moieties were synthesized and tested for their anti-bacterial activity. Some compounds presented great anti-microbial activities against Gram-positive bacteria (including
Ana Martinez et al.
Journal of medicinal chemistry, 48(23), 7103-7112 (2005-11-11)
The 2,4-disubstituted thiadiazolidinones (TDZD) are described as the first ATP-noncompetitive GSK-3 inhibitors. Following an SAR study about TDZD, different structural modifications in the heterocyclic ring aimed to test the influence of each heteroatom on the biological study are here reported
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