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2-Benzoylpyridine

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2-Benzoylpyridine Basic information

Product Name:
2-Benzoylpyridine
Synonyms:
  • ketone,phenyl2-pyridyl
  • Phenyl(2-pyridinyl)methanone
  • phenyl-2-pyridinyl-methanon
  • Pyridine, 2-benzoyl-
  • AKOS B022444
  • AKOS 94378
  • 2-BENZOYLPYRIDINE
  • PHENYL(PYRIDIN-2-YL)METHANONE
CAS:
91-02-1
MF:
C12H9NO
MW:
183.21
EINECS:
202-034-3
Product Categories:
  • Pyridines derivates
Mol File:
91-02-1.mol
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2-Benzoylpyridine Chemical Properties

Melting point:
41-43 °C (lit.)
Boiling point:
317 °C (lit.)
Density 
1,556 g/cm3
refractive index 
1.5880 (estimate)
Flash point:
302 °F
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
2.90±0.10(Predicted)
form 
Crystalline Chunks
color 
Colorless to slightly yellow
Water Solubility 
insoluble
BRN 
120283
LogP
1.880
CAS DataBase Reference
91-02-1(CAS DataBase Reference)
NIST Chemistry Reference
Methanone, phenyl-2-pyridinyl-(91-02-1)
EPA Substance Registry System
Methanone, phenyl-2-pyridinyl- (91-02-1)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
OB6400000
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29333999

MSDS

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2-Benzoylpyridine Usage And Synthesis

Chemical Properties

COLOURLESS TO SLIGHTLY YELLOW CRYSTALLINE CHUNKS

Uses

Organic synthesis.

Uses

2-Benzoylpyridine is used as a reagent to assist crosslinking in acrylic coating compounds in the polymers industry. 2-Benzoylpyridine is also a precursor for thioemicarbazone compounds that exhibit high cytotoxic activity against human leukemia cell lines and also posesses some antiinflammatory qualities.

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 24, p. 1061, 1987 DOI: 10.1002/jhet.5570240429
Tetrahedron Letters, 25, p. 1715, 1984 DOI: 10.1016/S0040-4039(01)81152-7

Purification Methods

Dissolve 2-benzoylpyridine in Et2O, shake it with aqueous NaHCO3, H2O, dry it over MgSO4 and evaporate. The residue solidifies on cooling. The solid can be recrystallised from pet ether. Its hydrochloride crystallises from Me2CO, m 126-127o, and the 2,4-dinitrophenylhydrazone has m 193-195o. It distils at high vacuum. [Kinkerton & Thames J Organomet Chem 24 623 1970, Beilstein 21/8 V 566.]

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