1,1'-Carbonothioyldi(2(1H)-pyridinone)

Names

[ Name ]:
1,1'-Carbonothioyldi(2(1H)-pyridinone)

[Synonym ]:
2(1H)-Pyridinone,1,1'-carbonothioylbis
2(1H)-Pyridinone, 1,1'-carbonothioylbis-
1,1'-Carbonothioyldi(2(1H)-pyridinone)
1,1′-Thiocarbonyldi-2(1H)-pyridone
N,N'-thiocarbonyldipyridone
1,1'-carbonothioyldipyridin-2(1H)-one
1,1'-Thiocarbonyldi-2(1H)-pyridone
1,1'-thiocarbonylbis(pyridin-2(1H)-one)
MFCD00075238

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
385.2±25.0 °C at 760 mmHg

[ Melting Point ]:
163-166ºC(lit.)

[ Molecular Formula ]:
C₁₁H₈N₂O₂S

[ Molecular Weight ]:
232.258

[ Flash Point ]:
186.8±23.2 °C

[ Exact Mass ]:
232.030655

[ PSA ]:
76.09000

[ LogP ]:
-0.67

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.720

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Excited-state intramolecular proton transfer distinguishes microenvironments in single- and double-stranded DNA.

J. Phys. Chem. B 112(38) , 12050-5, (2008)

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-hydroxych...

Phenethyl isothiocyanate and sulforaphane and their N-acetylcysteine conjugates inhibit malignant progression of lung adenomas induced by tobacco carcinogens in A/J mice.

Cancer Res. 65(18) , 8548-57, (2005)

We have shown previously that naturally occurring isothiocyanates derived from cruciferous vegetables and their N-acetylcysteine conjugates inhibit lung adenoma formation induced by tobacco carcinogen...

Synthesis and antibacterial activity of arylpiperazinyl oxazolidinones with diversification of the N-substituents.

Bioorg. Med. Chem. Lett. 14(15) , 3881-3, (2004)

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 thio...