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Key Documents

520411

Sigma-Aldrich

5-Bromo-2-nitropyridine

99%

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About This Item

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

Quality Level

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)
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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