2,6-Dichloro-3-nitropyridine
Names
[ CAS No. ]:
16013-85-7
[ Name ]:
2,6-Dichloro-3-nitropyridine
[Synonym ]:
6-Dichloro-3-nitropyridine
2,6-dichloro-3-nitro-pyridine
2,6-DICHLORO-3-NITROPYRIDINE
DICHLORONITROPYRIDINE
3-Nitro-2,6-dichloropyridine
EINECS 240-151-1
MFCD00006234
2,6-Dichloro-3-nitro
T6NJ BG CNW FG
Pyridine, 2,6-dichloro-3-nitro-
2,6-dicholoro-3-nitropyridine
2,6-Dichloro-3-nitropyrid...
PYRIDINE,2,6-DICHLORO-3-NITRO
Biological Activity
[Description]:
[Related Catalog]:
Chemical & Physical Properties
[ Density]:
1.6±0.1 g/cm3
[ Boiling Point ]:
295.5±35.0 °C at 760 mmHg
[ Melting Point ]:
55-60 °C(lit.)
[ Molecular Formula ]:
C5H2Cl2N2O2
[ Molecular Weight ]:
192.99
[ Flash Point ]:
132.5±25.9 °C
[ Exact Mass ]:
191.949326
[ PSA ]:
58.71000
[ LogP ]:
1.77
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.603
[ Storage condition ]:
Room temperature.
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H317-H319-H335
[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Faceshields;Gloves
[ Hazard Codes ]:
Xn,Xi
[ Risk Phrases ]:
R36/37/38:Irritating to eyes, respiratory system and skin . R42/43:May cause sensitization by inhalation and skin contact . R43:May cause sensitization by skin contact.
[ Safety Phrases ]:
S22-S26-S36/37-S37/39-S24
[ 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
Chem. Soc. Rev. 37(11) , 2393-402, (2008)
Oxacalix[n]arenes, reassessed members of the calixarene family in which the traditional methylene bridges are replaced by oxygen atoms, have emerged as a promising class of macrocycles in recent years...
Copper-mediated reaction of 2-halopyridines with ethyl bromodifluoroacetate. Ashwood MS, et al.Tetrahedron Lett. 43(50) , 9271-73, (2002)
Synthesis and functionalization of inherently chiral tetraoxacalix[2]arene[2]pyridines.
Org. Lett. 14(24) , 6254-7, (2012)
Inherently chiral tetraoxacalix[2]arene[2]pyridines containing C(2) symmetry were synthesized efficiently from a macrocyclic condensation reaction of resorcinol derivatives with 2,6-dichloro-3-nitropy...