2-Chloro-6-fluorobenzene-1-carbonyl chloride Property

Boiling point:

106 °C

Density 

1.43

refractive index 

1.525

Flash point:

93 °C

form 

clear liquid

color 

Colorless to Light yellow

Sensitive 

Moisture Sensitive

BRN 

4980867

CAS DataBase Reference

79455-63-3(CAS DataBase Reference)

Safety

Hazard Codes 

C

Risk Statements 

34

Safety Statements 

26-36/37/39-45

RIDADR 

3265

Hazard Note 

Corrosive

HazardClass 

8

PackingGroup 

II

HS Code 

29163990

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H227Combustible liquid

H290May be corrosive to metals

H314Causes severe skin burns and eye damage

H318Causes serious eye damage

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P234Keep only in original container.

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P330+P331IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P370+P378In case of fire: Use … for extinction.

P390Absorb spillage to prevent material damage.

P403+P235Store in a well-ventilated place. Keep cool.

P405Store locked up.

P406Store in corrosive resistant/… container with a resistant inner liner.

P501Dispose of contents/container to..…

2-Chloro-6-fluorobenzene-1-carbonyl chloride Chemical Properties,Usage,Production

Chemical Properties

Light yellow liquid

Source

2-Chloro-6-fluorobenzene-1-carbonyl chloride is a byproduct of the preparation process for 2-chloro-6-fluorobenzoic acid. In this process, 2-chloro-6-fluorobenzoic acid is prepared by refluxing the filtrate with thionyl chloride and dehydrating it with organic solvents. The amide product (2-chloro-6-fluoroaniline) is then reacted with an appropriate methylphenyl or methoxyphenyl to produce 2-Chloro-6-fluorobenzene-1-carbonyl chloride.