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B14000

Sigma-Aldrich

2-Benzoylpyridine

≥99%

Synonym(s):

Phenyl 2-pyridyl ketone

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About This Item

Empirical Formula (Hill Notation):
C12H9NO
CAS Number:
91-02-1
Molecular Weight:
183.21
Beilstein/REAXYS Number:
120283
EC Number:
202-034-3
MDL number:
MFCD00006300
UNSPSC Code:
12352100
PubChem Substance ID:
24891590
NACRES:
NA.22

assay

≥99%

form

crystals

bp

317 °C (lit.)

mp

41-43 °C (lit.)

SMILES string

O=C(c1ccccc1)c2ccccn2

InChI

1S/C12H9NO/c14-12(10-6-2-1-3-7-10)11-8-4-5-9-13-11/h1-9H

InChI key

GCSHUYKULREZSJ-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

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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Sigma-Aldrich

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Ahmed S M Al-Janabi et al.
Journal of molecular structure, 1228, 129454-129454 (2020-10-27)
New Schiff bases {N'-(phenyl(pyridin-2-yl)methylene) isonicotinohydrazide (L1H), N1 -(naphthalen-1-yl)-N2 -(phenyl(pyridin-2-yl) methylidene) ethane-1,2-diamine (L2H), N-(6-chlorobenzo[d]thiazol-2-yl)-1-phenyl-1-(pyridin-2-yl) methanimine (L3H)}were synthesized by reaction of 2-benzoylpyridine with different amines (2-amino-6-chlorobenzothiazole, isonicotinohydrazide and N 1-(naphthalen-1-yl)ethane-1,2-diamine) and characterized by 1H-NMR, 13C-NMR, IR mass spectroscopy and elemental analysis. The
Yu-Lan Li et al.
Anti-cancer agents in medicinal chemistry, 20(4), 504-517 (2019-11-14)
To overcome the disadvantages of cisplatin, numerous platinum (Pt) complexes have been prepared. However, the anticancer activity and mechanism of Pt(II) complexed with 2-benzoylpyridine [Pt(II)- Bpy]: [PtCl2(DMSO)L] (DMSO = dimethyl sulfoxide, L = 2-benzoylpyridine) in cancer cells remain unknown. Pt(II)-Bpy
Sandeep Kumar Dash et al.
Journal of applied toxicology : JAT, 34(11), 1130-1144 (2014-01-31)
The aim of the present study was to develop zinc sulfide nanoparticles (ZnS NPs) and to study their cytotoxicity against the KG-1A (human acute myeloid leukemia) cell line. ZnS NPs were synthesized using the pyrolytic method and characterized by X-ray

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