5-Bromo-2-nitropyridine

[Description]:

[Related Catalog]:

[ Density]:
1.8±0.1 g/cm3

[ Boiling Point ]:
292.3±20.0 °C at 760 mmHg

[ Melting Point ]:
148-150 °C(lit.)

[ Molecular Formula ]:
C₅H₃BrN₂O₂

[ Molecular Weight ]:
202.99

[ Flash Point ]:
130.6±21.8 °C

[ Exact Mass ]:
201.937775

[ PSA ]:
58.71000

[ LogP ]:
1.38

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.614

Click to get detail MSDS

[ 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 ]:
R36/37/38

[ Safety Phrases ]:
S26-S36/37

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ HS Code ]:
2933399090

Click to get detail synthetic route

Precursor

DownStream

[ 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%

A simple Cu-catalyzed coupling approach to substituted 3-pyridinol and 5-pyrimidinol antioxidants.

J. Org. Chem. 73(23) , 9326-33, (2008)

A convenient approach to 3-pyridinols and 5-pyrimidinols via a two-step Cu-catalyzed benzyloxylation/catalytic hydrogenation sequence is presented. The corresponding 3-pyridinamines and 5-pyrimidinami...

Structure-activity relationship study of EphB3 receptor tyrosine kinase inhibitors.

Bioorg. Med. Chem. Lett. 19 , 6122, (2009)

A structure-activity relationship study for a 2-chloroanilide derivative of pyrazolo[1,5-a]pyridine revealed that increased EphB3 kinase inhibitory activity could be accomplished by retaining the 2-ch...

FT-Raman and FT-IR spectra, vibrational assignments and density functional studies of 5-bromo-2-nitropyridine. Sundaraganesan N, et al.

Spectrochim. Acta A 61(13) , 2995-3001, (2005)

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