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2,2,3,3,4,4-hexafluoro-1,5-diiodopentane, a perfluorinated hydrocarbon with the molecular formula C5H8I2F6, is a chemical compound characterized by the presence of six fluorine atoms and two iodine atoms attached to a five-carbon chain. It is known for its strong hydrophobic and lipophobic properties due to its highly fluorinated nature, making it a versatile reagent in various applications.

33619-80-6

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33619-80-6 Usage

Uses

Used in Organic Synthesis:
2,2,3,3,4,4-hexafluoro-1,5-diiodopentane is used as a reagent in organic synthesis for introducing fluorine and iodine atoms into organic molecules. Its unique structure allows for the creation of new compounds with specific properties, making it valuable in the development of novel materials and pharmaceuticals.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,2,3,3,4,4-hexafluoro-1,5-diiodopentane is utilized as a key intermediate in the synthesis of various drugs. Its ability to introduce fluorine and iodine atoms into organic molecules contributes to the development of new therapeutic agents with improved pharmacological properties.
Used in Agrochemicals:
2,2,3,3,4,4-hexafluoro-1,5-diiodopentane is also employed in the production of agrochemicals, where its reactivity and fluorine-containing properties are leveraged to create new pesticides or herbicides with enhanced efficacy and selectivity.
Used in Materials Science:
In materials science, 2,2,3,3,4,4-hexafluoro-1,5-diiodopentane is used as a building block for the development of advanced materials with unique properties. Its hydrophobic and lipophobic characteristics make it suitable for applications in coatings, lubricants, and other materials that require non-reactivity with other compounds.
It is crucial to handle 2,2,3,3,4,4-hexafluoro-1,5-diiodopentane with care, as it is potentially hazardous if not used properly. Proper safety measures and precautions should be taken during its synthesis, storage, and application to ensure the safety of both the environment and the individuals involved in its use.

Check Digit Verification of cas no

The CAS Registry Mumber 33619-80-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,1 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33619-80:
(7*3)+(6*3)+(5*6)+(4*1)+(3*9)+(2*8)+(1*0)=116
116 % 10 = 6
So 33619-80-6 is a valid CAS Registry Number.

33619-80-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,4,4-hexafluoro-1,5-diiodopentane

1.2 Other means of identification

Product number -
Other names 2,2,3,3,4,4-hexafluoro-1,5-diiodo-pentane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33619-80-6 SDS

33619-80-6Downstream Products

33619-80-6Relevant academic research and scientific papers

Reductive dehalogenation of polyhalofluorocarbons with tributyltin hydride

Puy, Michael Van Der,Belter, Randolph K.,Borowski, Ralph J.,Ellis, Lois A. S.,Persichini, Phillip J.,et al.

, p. 59 - 64 (2007/10/02)

The reduction of polyhalofluorocarbons, including ClCF2CFClCF2Cl, (ClCF2CFCl)2, ICH2(CF2)3CH2I and vicinal dichloroperfluorocycloalkanes, with tributyltin hydride gave the corresponding hydrofluorocarbons in good to excellent yield.The results are compared with similar reductions with other reducing agents, and to tin hydride reductions of non-fluorinated analogs. - Keywords: Reductive dehalogenation; Polyfluorocarbons; Tributyltin hydride; NMR spectroscopy; Hydrofluorocarbons

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