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3-Pyridinecarbonitrile, 1,2-dihydro-6-methyl-2-oxo-5-phenyl- (9CI)

Names

[ CAS No. ]:
4241-12-7

[ Name ]:
3-Pyridinecarbonitrile, 1,2-dihydro-6-methyl-2-oxo-5-phenyl- (9CI)

[Synonym ]:
NICOTINONITRILE,2-HYDROXY-6-METHYL-5-PHENYL
6-methyl-2-oxo-5-phenyl-1,2-dihydro-3-pyridinecarbonitrile
2-Hydroxy-6-methyl-5-phenylnicotinonitrile
3-cyano-6-methyl-5-phenyl-1H-pyridin-2-one
3-Pyridinecarbonitrile,2-hydroxy-6-methyl-5-phenyl
3-cyano-6-methyl-5-phenyl-2-pyridone
6-methyl-5-phenylpyrid-2-one-3-carbonitrile
3-cyano-5-phenyl-6-methyl-1,2-dihydropyrid-2-one
3-Pyridinecarbonitrile,2-dihydro-6-methyl-2-oxo-5-phenyl
6-methyl-2-oxo-5-phenyl-1,2-dihydropyridine-3-carbonitrile

Chemical & Physical Properties

[ Density]:
1.22g/cm3

[ Boiling Point ]:
417.4ºC at 760 mmHg

[ Molecular Formula ]:
C13H10N2O

[ Molecular Weight ]:
210.23100

[ Flash Point ]:
206.3ºC

[ Exact Mass ]:
210.07900

[ PSA ]:
56.65000

[ LogP ]:
2.22198

[ Index of Refraction ]:
1.618

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
QT3230000
CHEMICAL NAME :
Nicotinonitrile, 2-hydroxy-6-methyl-5-phenyl-
CAS REGISTRY NUMBER :
4241-12-7
LAST UPDATED :
197901
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C13-H10-N2-O
MOLECULAR WEIGHT :
210.25
WISWESSER LINE NOTATION :
T6NJ BQ CCN ER& F1

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
320 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) Volume(issue)/page/year: NX#02428

Safety Information

[ HS Code ]:
2933399090

Precursor & DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%


Related Compounds