<Suppliers Price>

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]:

2,6-Dichloro-3-nitropyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

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

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

Oxacalix[n](het)arenes.

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...


More Articles


Related Compounds