Ethyl 6-chloronicotinate
Names
[ CAS No. ]:
49608-01-7
[ Name ]:
Ethyl 6-chloronicotinate
[Synonym ]:
Ethyl 6-chloronicotinate
T6NJ BG EVO2
2-Chloro-5-pyridinecarboxylic Acid Ethyl Ester
Ethyl 2-Chloro-5-pyridinecarboxylate
6-Chloro-3-pyridinecarboxylic acid ethyl ester
ethyl 6-chloropyridine-3-carboxylate
6-Chloronicotinic acid ethyl ester
Ethyl 6-chloro-3-pyridinecarboxylate
MFCD00082739
3-Pyridinecarboxylic acid, 6-chloro-, ethyl ester
Chemical & Physical Properties
[ Density]:
1.2±0.1 g/cm3
[ Boiling Point ]:
249.2±20.0 °C at 760 mmHg
[ Melting Point ]:
26-30 °C(lit.)
[ Molecular Formula ]:
C8H8ClNO2
[ Molecular Weight ]:
185.608
[ Flash Point ]:
104.5±21.8 °C
[ Exact Mass ]:
185.024353
[ PSA ]:
39.19000
[ LogP ]:
2.05
[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C
[ Index of Refraction ]:
1.525
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-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2933399090
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
Org. Lett. 16(7) , 2018-21, (2014)
Lanthanum trifluoromethanesulfonate is an effective single-component catalyst for synthesizing a variety of amides directly from esters and amines under mild conditions. Highly selective amidation of ...
The spectroscopic (FT-IR, FT-Raman, dispersive Raman and NMR) study of ethyl-6-chloronicotinate molecule by combined density functional theory. Karabacak M, et al.Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 153 , 754-770, (2016)
Microwave-assisted Sonogashira coupling of novel 2-[6-(arylethynyl) pyridin-3-yl]-1H-benzimidazole derivatives. Raut CN, et al.
ARKIVOC 11 , 105-114, (2009)