347558
4-Oxo-2-thioxo-3-thiazolidinylacetic acid
≥99%
Synonym(s):
Rhodanine-3-acetic acid
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C5H5NO3S2
CAS Number:
Molecular Weight:
191.23
Beilstein/REAXYS Number:
149513
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
assay
≥99%
form
solid
mp
145-148 °C (lit.)
solubility
methanol: soluble 25 mg/mL, clear, yellow
functional group
carboxylic acid
thioether
SMILES string
OC(=O)CN1C(=O)CSC1=S
InChI
1S/C5H5NO3S2/c7-3-2-11-5(10)6(3)1-4(8)9/h1-2H2,(H,8,9)
InChI key
JGRMXPSUZIYDRR-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
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_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service