2-Chloronicotinamide
Names
[ CAS No. ]:
10366-35-5
[ Name ]:
2-Chloronicotinamide
[Synonym ]:
3-Pyridinecarboxamide,2-chloro
chloro-2 amido-3 pyridine
2-chloro-3-pyridinecarboxamide
2-Chloronicotinamide
chloronicotinamide
2-Chlorpyridin-3-carboxamid
2-CHLORO-PYRIDIN-3-CARBOXYLIC ACID AMIDE
3-Pyridinecarboxamide, 2-chloro-
2-CHLORONICOTINAMIDE CNAM
2-Chloropyridine-3-Carboxamide
RARECHEM AH CK 0070
EINECS 233-808-9
2-CHLORONICOTINALDEHYDE
MFCD00006237
2-chloro-nicotinic acid amide
Chemical & Physical Properties
[ Density]:
1.4±0.1 g/cm3
[ Boiling Point ]:
313.7±27.0 °C at 760 mmHg
[ Melting Point ]:
164-167 °C(lit.)
[ Molecular Formula ]:
C6H5ClN2O
[ Molecular Weight ]:
156.570
[ Flash Point ]:
143.5±23.7 °C
[ Exact Mass ]:
156.009033
[ PSA ]:
55.98000
[ LogP ]:
0.16
[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C
[ Index of Refraction ]:
1.589
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi:Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2933399090
Synthetic Route
Precursor & DownStream
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%
Articles
Infect. Immun. 38(2) , 548-53, (1982)
Several conditions of growth of Bordetella pertussis cause a reversible phenotypic alteration in properties termed modulation. Growth in medium containing nicotinic acid induces normal (X-mode) cells ...
Microwave assisted copper-free Sonogashira coupling/5-exo-dig cycloisomerization domino reaction: access to 3-(phenylmethylene) isoindolin-1-ones and related heterocycles. Hellal M and Cuny GD.Tetrahedron Lett. 52(42) , 5508-11, (2011)
Benzyl and tert Butyl Sulfoxides as Sulfenyl Halide Equivalents: a Convenient Preparation of Benzisothiazolones. Wright SW, et al.
Tetrahedron Lett. 33 , 153-6, (1992)