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Merck
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文件

520411

Sigma-Aldrich

5-溴-2-硝基吡啶

99%

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About This Item

经验公式（希尔记法）:
C5H3BrN2O2
CAS号:
39856-50-3
分子量:
202.99
MDL號碼:
MFCD00160411
分類程式碼代碼:
12352100
PubChem物質ID:
24874130
NACRES:
NA.22

化驗

99%

mp

148-150 °C (lit.)

SMILES 字串

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

InChI

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

InChI 密鑰

ATXXLNCPVSUCNK-UHFFFAOYSA-N

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相关类别

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

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)
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
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)
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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