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341673

Sigma-Aldrich

1,1′-Thiocarbonyldi-2(1H)-pyridone

97%

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About This Item

Fórmula empírica (notación de Hill):
C11H8N2O2S
Número de CAS:
102368-13-8
Peso molecular:
232.26
MDL number:
MFCD00075238
UNSPSC Code:
12352100
PubChem Substance ID:
24860980
NACRES:
NA.22

Quality Level

100

assay

97%

mp

163-166 °C (lit.)

SMILES string

O=C1C=CC=CN1C(=S)N2C=CC=CC2=O

InChI

1S/C11H8N2O2S/c14-9-5-1-3-7-12(9)11(16)13-8-4-2-6-10(13)15/h1-8H

InChI key

KXMMNJQMGILZDB-UHFFFAOYSA-N

Application

1,1′-Thiocarbonyldi-2(1H)-pyridone was used in the preparation of:
  • thio-analogs of thioureas
  • sulforaphane
  • 2-furan-2-yl-3-hydroxy-6-isothiocyanato-chromen-4-one

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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

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C Clifford Conaway et al.
Cancer research, 65(18), 8548-8557 (2005-09-17)
We have shown previously that naturally occurring isothiocyanates derived from cruciferous vegetables and their N-acetylcysteine conjugates inhibit lung adenoma formation induced by tobacco carcinogens in A/J mice at the post-initiation stage. The tumor-inhibitory activity by these compounds is linked with
Sun-Young Jang et al.
Bioorganic & medicinal chemistry letters, 14(15), 3881-3883 (2004-07-01)
A series of 4-arylpiperazin-1-yl-3-phenyloxazolidin-2-one derivatives with diversification of the N-substituents such as methylene O-linked heterocycles, thioamide, dithiocarbamate, thiourea, and thiocarbamate were synthesized and evaluated as antibacterial agents. Their in vitro activities (MIC) were evaluated against MRSA and VRE resistant Gram-positive
Andrey S Klymchenko et al.
The journal of physical chemistry. B, 112(38), 12050-12055 (2008-09-05)
Herein, the efficient interaction of an environment-sensitive fluorophore that undergoes excited-state intramolecular proton transfer (ESIPT) with DNA has been realized by conjugation of a 3-hydroxychromone (3HC) with polycationic spermine. On binding to a double-stranded DNA (dsDNA), the ratio of the

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