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05594

Supelco

6-Phenyl-2-thiouracil

analytical standard

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About This Item

Fórmula empírica (Notação de Hill):
C10H8N2OS
Número CAS:
Peso molecular:
204.25
Número CE:
Número MDL:
Código UNSPSC:
41116107
ID de substância PubChem:
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

Ensaio

≥97.5% (HPLC)
≥97.5% (NT)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

clinical testing

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

Oc1cc(nc(S)n1)-c2ccccc2

InChI

1S/C10H8N2OS/c13-9-6-8(11-10(14)12-9)7-4-2-1-3-5-7/h1-6H,(H2,11,12,13,14)

chave InChI

XEKNACRTWJHOCE-UHFFFAOYSA-N

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Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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R Schilt et al.
Journal of chromatography, 489(1), 127-137 (1989-04-07)
Methods are described for the screening and confirmation of residues of the thyreostatics thiouracil, methylthiouracil and propylthiouracil in urine samples of cattle at levels down to 25 micrograms/l. After a selective preconcentration of the thiol-containing thyreostatics on a mercurated affinity
X Huang et al.
Journal of molecular and cellular cardiology, 32(12), 2221-2228 (2000-12-13)
Two main troponin I genes, cardiac (cTnI) and slow skeletal (ssTnI), are expressed in the mammalian heart under the control of a developmentally regulated program. ssTnI is expressed first in embryonic and fetal heart, and is then downregulated by an
Tomás Pérez-Ruiz et al.
Electrophoresis, 26(12), 2384-2390 (2005-05-17)
This paper reports the development of a method based on capillary electrophoresis with laser-induced fluorescence detection for the simultaneous determination of thiouracil (TU) and phenylthiouracil (PhTU) with high sensitivity (nanomolar range, i.e., attomoles detected). After derivatization with 5-iodoacetamidofluorescein, the analytes
Highly potent and selective inhibition of HIV-1 replication by 6-phenylthiouracil derivatives.
M Baba et al.
Antiviral research, 17(4), 245-264 (1992-04-01)

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