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Merck
CN

R1102

4-Oxo-2-thioxo-3-thiazolidinylacetic acid

95%

Synonym(s):

Rhodanine-3-acetic acid

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About This Item

Empirical Formula (Hill Notation):
C5H5NO3S2
CAS Number:
Molecular Weight:
191.23
EC Number:
227-220-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
149513
MDL number:
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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

95%

mp

145-148 °C (lit.)

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

Regulatory Information

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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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