1,1'-Carbonothioyldi(2(1H)-pyridinone)
Names
[ CAS No. ]:
102368-13-8
[ 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
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
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...