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2,6-Dichloro-3-trifluoromethylpyridine

Names

[ CAS No. ]:
55304-75-1

[ Name ]:
2,6-Dichloro-3-trifluoromethylpyridine

[Synonym ]:
2,6-dichloro-5-trifluoromethylpyridine
MFCD00042245
2,6-Dichloro-3-(trifluoromethyl)pyridine
Pyridine, 2,6-dichloro-3-(trifluoromethyl)-
EINECS 259-585-8
2,6-Dichloro-3-trifluoromethylpyridine
2,5-DIBENZYL-6A-METHYL-HEXAHYDRO-PENTALENE-3A-CARBOXYLIC ACID ETHYL ESTER
2,6-dichloronicotinonitrile

Chemical & Physical Properties

[ Density]:
1.5±0.1 g/cm3

[ Boiling Point ]:
221.0±35.0 °C at 760 mmHg

[ Melting Point ]:
194 °C

[ Molecular Formula ]:
C6H2Cl2F3N

[ Molecular Weight ]:
215.988

[ Flash Point ]:
87.5±25.9 °C

[ Exact Mass ]:
214.951645

[ PSA ]:
12.89000

[ LogP ]:
3.27

[ Vapour Pressure ]:
0.2±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.470

MSDS

Safety Information

[ Symbol ]:

GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H300-H315-H319-H335

[ Precautionary Statements ]:
P261-P264-P301 + P310-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
T:Toxic;

[ Risk Phrases ]:
R25;R36/37/38

[ Safety Phrases ]:
S26-S36/37-S45

[ RIDADR ]:
UN 2810 6.1/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ 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%

Articles

A practical preparation of methyl 2-methoxy-6-methylaminopyridine-3-carboxylate from 2,6-dichloro-3-trifluoromethylpyridine.

Chem. Pharm. Bull. 49(12) , 1621-7, (2001)

An effective and practical synthetic route to methyl 2-methoxy-6-methylaminopyridine-3-carboxylate (7), the key intermediate of 5-bromo-2-methoxy-6-methylaminopyridine-3-carboxylic acid (1), from 2,6-...


More Articles


Related Compounds

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