672339-38-7

Basic information

• Product Name: 2,3,3,3-TETRAFLUORO-1-IODOPROPENE
• Synonyms: 2,3,3,3-TETRAFLUORO-1-IODOPROPENE
• CAS NO: 672339-38-7
• Molecular Formula: C₃HF₄I
• Molecular Weight: 239.94
• Mol File: 672339-38-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 55.6°C at 760 mmHg
• Flash Point: 9.8°C
• Appearance: /
• Density: 2.139g/cm³
• Vapor Pressure: 248mmHg at 25°C
• Refractive Index: 1.438
• CAS DataBase Reference: 2,3,3,3-TETRAFLUORO-1-IODOPROPENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,3,3-TETRAFLUORO-1-IODOPROPENE(672339-38-7)
• EPA Substance Registry System: 2,3,3,3-TETRAFLUORO-1-IODOPROPENE(672339-38-7)

Safety Data

• Hazardous Substances Data: 672339-38-7(Hazardous Substances Data)

Usage

Physical state

Colorless liquid

Odor

Strong

Uses

Industrial applications (pharmaceuticals, agrochemicals, specialty materials), building block in organic synthesis

Reactivity

Highly reactive and versatile reagent

Safety precautions

Toxic and flammable, can cause skin and eye irritation

InChI:InChI=1/C3HF4I/c4-2(1-8)3(5,6)7/h1H/b2-1+

Upstream product

• 354-69-8 2,2,3,3,3-pentafluoro-n-propyl iodide 

Downstream Products

• 130654-80-7 1-methoxy-2-(3,3,3-trifluoroprop-1-yn-1-yl)benzene 
• 573979-96-1 ethyl 4-(3,3,3-trifluoroprop-1-yn-1-yl)benzoate 

Relevant articles and documents

Highly stereoselective approach to 3-fluoroalkylated (E)-hex-3-ene-1,5- diyne derivatives via an addition-elimination reaction

Palladium(0)-catalyzed Sonogashira cross-coupling reaction of 2-fluoroalkylated (Z)-2-fluoro-1-iodoethene, which is easily prepared from commercially available polyfluorinated alcohols in facile three steps, with terminal alkynes in DMF at room temperature for 24 h took place stereospecifically to give the corresponding 1-fluoroalkylated (Z)-1-fluorobut-1-en-3-yne derivatives in good to excellent yield. Thus obtained fluoroalkylated 1-fluoroenynes were effectively subjected to addition-elimination reaction with various alkynyllithiums at room temperature, leading to 3-fluoroalkylated hex-3-ene-1,5-diyne derivatives in good to high yields with an excellent E selectivity.