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520411

Sigma-Aldrich

5-Bromo-2-nitropyridine

99%

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About This Item

Empirical Formula (Hill Notation):
C5H3BrN2O2
CAS Number:
39856-50-3
Molecular Weight:
202.99
MDL number:
MFCD00160411
UNSPSC Code:
12352100
PubChem Substance ID:
24874130
NACRES:
NA.22

assay

99%

mp

148-150 °C (lit.)

SMILES string

[O-][N+](=O)c1ccc(Br)cn1

InChI

1S/C5H3BrN2O2/c6-4-1-2-5(7-3-4)8(9)10/h1-3H

InChI key

ATXXLNCPVSUCNK-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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FT-Raman and FT-IR spectra, vibrational assignments and density functional studies of 5-bromo-2-nitropyridine.
Sundaraganesan N, et al.
Spectrochimica Acta Part A: Molecular Spectroscopy, 61(13), 2995-3001 (2005)
Synthesis of fluorine-18-labelled 5-and 6-fluoro-2-pyridinamine.
Abrahim A, et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 49(4), 345-356 (2006)
Structure-based design and synthesis of the first weak non-phosphate inhibitors for IspF, an enzyme in the non-mevalonate pathway of isoprenoid biosynthesis.
Baumgartner C, et al.
Helvetica Chimica Acta, 90(6), 1043-1068 (2007)
Lixin Qiao et al.
Bioorganic & medicinal chemistry letters, 19(21), 6122-6126 (2009-09-29)
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-chloroanilide and introducing a phenyl or small electron donating substituents to the 5-position of the pyrazolo[1,5-a]pyridine. In
Susheel J Nara et al.
The Journal of organic chemistry, 73(23), 9326-9333 (2008-11-04)
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-pyrimidinamines can be prepared in an analogous sequence utilizing benzylamine in lieu of benzyl alcohol. The radical-scavenging ability of these

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