216144-70-6

Basic information

• Product Name: 5-FLUORO-2-(TRIFLUOROMETHYL)BENZOYL CHLORIDE
• Synonyms: OTF-BOC-5F;2-TRIFLUOROMETHYL-5-FLUOROBENZOYL CHLORIDE;5-FLUORO-2-(TRIFLUOROMETHYL)BENZOYL CHLORIDE;alpha,alpha,alpha,5-Tertafluoro-o-toluoyl chloride;à,à,à,5-tertafluoro-o-toluoyl chloride;5-Fluoro-2-(trifluoromethyl)benzoyl chloride 97%;5-Fluoro-2-(trifluoromethyl)benzoylchloride97%;alpha,alpha,alpha,5-Tetrafluoro-o-toluoyl Chloride
• CAS NO: 216144-70-6
• Molecular Formula: C8H3ClF4O
• Molecular Weight: 226.56
• EINECS: -0
• Product Categories: Acid Halides;Carbonyl Compounds;Organic Building Blocks
• Mol File: 216144-70-6.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 169 °C(lit.)
• Flash Point: 188 °F
• Appearance: /
• Density: 1.5 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.166mmHg at 25°C
• Refractive Index: n20/D 1.463(lit.)
• Storage Temp.: Inert atmosphere,Room Temperature
• Sensitive: Moisture Sensitive
• CAS DataBase Reference: 5-FLUORO-2-(TRIFLUOROMETHYL)BENZOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-FLUORO-2-(TRIFLUOROMETHYL)BENZOYL CHLORIDE(216144-70-6)
• EPA Substance Registry System: 5-FLUORO-2-(TRIFLUOROMETHYL)BENZOYL CHLORIDE(216144-70-6)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 23-26-36/37/39-45
• RIDADR: UN 3265 8/PG 2
• WGK Germany: 3
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 216144-70-6(Hazardous Substances Data)

Usage

General Description

5-Fluoro-2-(trifluoromethyl)benzoyl chloride is a chemical compound consisting of a benzene ring with a fluorine atom at the 5th position and a trifluoromethyl group attached to the 2nd position, as well as a benzoyl chloride functional group. 5-Fluoro-2-(trifluoromethyl)benzoyl chloride is often used as a reagent in organic synthesis, specifically in the preparation of various pharmaceuticals and agrochemicals. It is a versatile building block in the creation of complex molecules and can participate in a variety of chemical reactions, including acylation and nucleophilic substitution. Its unique structure and reactivity make it a valuable tool in the field of synthetic chemistry.

InChI:InChI=1/C8H3ClF4O/c9-7(14)5-3-4(10)1-2-6(5)8(11,12)13/h1-3H