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38565-62-7

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38565-62-7 Usage

Description

Dodecane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodois a synthetic fluorinated compound with the chemical formula C12H21F17I. It is a halogenated organic compound that consists of twelve carbon atoms and seventeen fluorine atoms, with an iodine atom attached to the 12th carbon. Dodecane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodois characterized by its unique structure and properties, making it a valuable reagent in chemical synthesis.

Uses

Used in Chemical Synthesis:
Dodecane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodois used as a fluorine-containing reagent in chemical synthesis for the production of more complex molecules. Its unique structure allows for versatile reactions and the formation of a wide range of compounds.
Used in Specialty Chemicals Production:
Dodecane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodois utilized in the production of specialty chemicals, which are high-value chemicals used in various industries. Its unique properties make it suitable for creating specialty chemicals with specific characteristics and applications.
Used in Pharmaceutical Industry:
Dodecane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodohas potential applications in the pharmaceutical industry, where it can be used as a building block for the development of new drugs or as a reagent in the synthesis of pharmaceutical compounds.
Used in Agrochemicals Industry:
In the agrochemicals industry, this compound may be used for the development of new agrochemical products, such as pesticides or herbicides, due to its unique properties and reactivity.
Used in Materials Science:
Dodecane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodomay also have applications in materials science, where it can be used to develop new materials with specific properties, such as high thermal stability or chemical resistance.
Used for Research and Development:
Dodecane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodo-'s unique structure and properties make it useful for research and development purposes in various fields, including chemistry, materials science, and pharmaceuticals. It can be employed to explore new reaction pathways, develop novel synthesis methods, or study the properties of fluorinated compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 38565-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,5,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38565-62:
(7*3)+(6*8)+(5*5)+(4*6)+(3*5)+(2*6)+(1*2)=147
147 % 10 = 7
So 38565-62-7 is a valid CAS Registry Number.

38565-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodododecane

1.2 Other means of identification

Product number -
Other names Dodecane,1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-12-iodo

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:38565-62-7 SDS

38565-62-7Relevant articles and documents

Coupling between a fluorinated olefin and a perfluorinated iodide: A model study on the reaction mechanism of perfluorinated polymer cross-linking

Wlassics, Ivan,Barchiesi,Sala

, p. 119 - 126 (2003)

In a model study, 1H, 19C, 13 C-1H and 1H-1H correlated NMR techniques confirm a Markovnikov type reaction intermediate for the major coupling products between a short, low MW perfluorinated iodide C2F5I (I) and a short, low MW fluorinated olefin CF3(CF2)7CH=CH2 (II). The reaction is peroxide induced (di-t-butyl peroxide, DTBP) and is conducted at 140 °C for a 3 h reaction time in a sealed glass ampoule. Side reaction products due to the reaction of DTBP with radical reaction intermediates were also observed and identified. The study aimed to mimic as closely as possible the peroxide-initiated coupling reaction between an iodine terminated fluoropolymer (model compound I) and its fluorinated di-olefin coupling agent (model compound II). A mono-olefin was chosen to simplify the model reaction.

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