ChemicalBook--->CAS DataBase List--->69045-78-9

69045-78-9

69045-78-9 Structure

69045-78-9 Structure
IdentificationMore
[Name]

2-Chloro-5-trichloromethylpyridine
[CAS]

69045-78-9
[Synonyms]

2-CHLORO-5-TRICHLOROMETHYL PYRIDINE
AKOS BBS-00000412
IFLAB-BB F0797-0001
[EINECS(EC#)]

614-911-1
[Molecular Formula]

C6H3Cl4N
[MDL Number]

MFCD00160145
[Molecular Weight]

230.91
[MOL File]

69045-78-9.mol
Chemical PropertiesBack Directory
[Melting point ]

-18.14 °C
[Boiling point ]

281.8±35.0 °C(Predicted)
[density ]

1.582±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

solid
[pka]

-2.26±0.10(Predicted)
[color ]

Pink
[CAS DataBase Reference]

69045-78-9(CAS DataBase Reference)
[EPA Substance Registry System]

69045-78-9(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P260-P280-P312
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
[RIDADR ]

UN2811
[Hazard Note ]

Irritant
[TSCA ]

TSCA listed
[HS Code ]

2933399990
Raw materials And Preparation ProductsBack Directory
[Preparation Products]

Fluazifop-P-butyl-->2-Chloro-5-trifluoromethylpyridine-->2-Chloro-5-(chloromethyl)pyridine-->2,3-Dichloro-5-(trifluoromethyl)pyridine-->Fluazifop-butyl
Spectrum DetailBack Directory
[Spectrum Detail]

2-Chloro-5-trichloromethylpyridine(69045-78-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

A synthetic method of 2-chloro-5-trichloromethyl pyridine comprises the following steps of (1) synthesis of N-oxygen-3-methylpyridine: reacting by taking 3-methylpyridine as a raw material, glacial acetic acid as a solvent and 60% hydrogen peroxide as an oxidizing agent to obtain N-oxygen-3-methylpyridine; (2) synthesis of 2-chloro-5-methylpyridine: carrying out oriented chlorination on N-oxygen-3-methylpyridine by taking benzoyl chloride as a chlorinating agent to obtain 2-chloro-5-methylpyridine; (3) synthesis of 2-chloro-5-trichloromethyl pyridine: reacting by taking methyl ethyl ketone peroxide as an initiating agent to obtain a crude 2-chloro-5-trichloromethyl pyridine product; (4) refining of 2-chloro-5-trifluoromethyl pyridine: carrying out halogen exchange fluoridation reaction by taking excessive potassium fluoride as a fluorizating agent, dimethyl sulfoxide as a solvent and hexadecyl trimethyl ammonium bromide as a phase transfer catalyst, and rectifying and purifying to obtain a fine 2-chloro-5-trichloromethyl pyridine product.
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