678-13-7

Basic information

• Product Name: 1,2-DICHLORO-4-IODOPERFLUOROBUTANE
• Synonyms: 1,2-DICHLORO-4-IODOPERFLUOROBUTANE
• CAS NO: 678-13-7
• Molecular Formula: C4Cl2F7I
• Molecular Weight: 378.8420924
• Mol File: 678-13-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 66°C 67mm
• Flash Point: 40.682°C
• Appearance: /
• Density: 2.171g/cm³
• Vapor Pressure: 6.636mmHg at 25°C
• Refractive Index: 1.421
• CAS DataBase Reference: 1,2-DICHLORO-4-IODOPERFLUOROBUTANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DICHLORO-4-IODOPERFLUOROBUTANE(678-13-7)
• EPA Substance Registry System: 1,2-DICHLORO-4-IODOPERFLUOROBUTANE(678-13-7)

Safety Data

• Hazardous Substances Data: 678-13-7(Hazardous Substances Data)

Usage

Description

1,2-Dichloro-4-iodoperfluorobutane is a perfluorinated chemical compound characterized by the presence of two chlorine atoms and one iodine atom attached to a four-carbon fluorinated chain. It is renowned for its unique properties such as high chemical stability and low reactivity with other substances, making it a valuable reagent in organic synthesis and a building block for pharmaceutical and agrochemical products.

Uses

Used in Organic Synthesis:
1,2-Dichloro-4-iodoperfluorobutane is used as a reagent in organic synthesis for its unique properties that facilitate the creation of various complex organic molecules.
Used in Pharmaceutical and Agrochemical Production:
1,2-DICHLORO-4-IODOPERFLUOROBUTANE serves as a building block in the development of pharmaceutical and agrochemical products, contributing to the synthesis of new and effective drugs and pesticides.
Used as a Solvent:
Due to its chemical stability, 1,2-dichloro-4-iodoperfluorobutane is utilized as a solvent in certain chemical processes where its inertness is advantageous.
Used in Specialty Chemicals Production:
It is employed as a starting material in the production of specialty chemicals, where its unique structure and properties are essential for the synthesis of specific compounds.
It is crucial to handle 1,2-dichloro-4-iodoperfluorobutane with care due to its toxic nature and potential hazards to human health and the environment.

InChI:InChI=1/C4Cl2F7I/c5-1(7,3(6,10)11)2(8,9)4(12,13)14

Upstream product

• 116-14-3 polytetrafluoroethylene 
• 354-61-0 1,2-dichloro-1,2,2-trifluoro-1-iodoethane 

Downstream Products

• 685-63-2 hexafluoro-1,3-butadiene 
• 357-21-1 3,4-dichlorohexafluoro-1-butene 
• 680-54-6 4-H-heptafluoro-1-butene 
• 14671-64-8 1,2-dichloro-1,1,2,3,3,4,4-heptafluoro-butane 
• 760-42-9 1,1,1,2,4,4,4-heptafluoro-2-butene 
• 1737-54-8 (3,4-Dichlor-heptafluorbutyl)-benzol 
• 55260-70-3 1,2-Dichlor-1,1,2,3,3,4,4,5,5,6-decafluor-6-iodhexan 
• 55260-69-0 1,2-Dichlor-1,1,2,3,3,4,4,5,6,6-decafluor-6-iodhexan 
• 14160-49-7 p-Bis-(3,4-dichlor-heptafluorbutyl)-benzol 
• 2450-01-3 1,2-Dichlor-6-jod-5,5,6,6-tetrahydro-perfluor-hexan 

Relevant articles and documents

New ring-containing fluoropolymers

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Process for preparing perhalogenated olefins

The invention relates to a process for preparing perhalogenated olefins which comprises reacting a perhalogenated alkane, having at least one atom of a halogen different from fluorine, with a tris-dialkylamino phosphine at temperature not higher than 60° C.

Process for preparing perhalogenated olefins

The invention relates to a process for preparing perhalogenated olefins which comprises reacting a perhalogenated alkane, having at least one atom of a halogen different from fluorine, with a tris-dialkylamino phosphine at temperature not higher than 60°C.