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Merck
모든 사진(1)

문서

347558

Sigma-Aldrich

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

≥99%

동의어(들):

Rhodanine-3-acetic acid

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C5H5NO3S2
CAS Number:
5718-83-2
Molecular Weight:
191.23
Beilstein:
149513
EC Number:
227-220-1
MDL number:
MFCD00005491
UNSPSC 코드:
12352100
PubChem Substance ID:
24861511
NACRES:
NA.22

Quality Level

100

분석

≥99%

형태

solid

mp

145-148 °C (lit.)

solubility

methanol: soluble 25 mg/mL, clear, yellow

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves

시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리 방문

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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