1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13-Heptacosafluoro-13-iodotridecane is a complex organic compound characterized by its molecular formula C13HF27I. 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13-Heptacosafluoro-13-iodotridecane is composed of a 13-carbon chain with 27 fluorine atoms and one iodine atom. The fluorine atoms are distributed across the carbon chain, with each carbon atom bonded to three fluorine atoms, except for the terminal carbon atoms, which are bonded to two fluorine atoms and one iodine atom. 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13-Heptacosafluoro-13-iodotridecane is highly fluorinated, which contributes to its unique chemical and physical properties, such as increased stability and resistance to chemical reactions. Due to its specific structure and composition, it may have potential applications in specialized fields such as high-performance materials or chemical research.
The CAS Registry Mumber 376-04-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 6 respectively; the second part has 2 digits, 0 and 4 respectively. Calculate Digit Verification of CAS Registry Number 376-04: (5*3)+(4*7)+(3*6)+(2*0)+(1*4)=65 65 % 10 = 5 So 376-04-5 is a valid CAS Registry Number.
376-04-5SDS
SAFETY DATA SHEETS
According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition
376-04-5Relevant academic research and scientific papers
Metal-free efficient, general and facile iododecarboxylation method with biodegradable co-products
Kulbitski, Kseniya,Nisnevich, Gennady,Gandelman, Mark
supporting information; experimental part, p. 1438 - 1442 (2011/07/30)
The development of a novel, efficient and robust method for the general conversion of aliphatic and aromatic carboxylic acids to organic iodides without the use of heavy metals or strong oxidizing agents is reported. Commercially available N-iodoamides were used for both initiation and halogen donation under irradiative conditions. Isolation of the product is extremely simple and the major co-product is removed as a water-soluble biodegradable material. Copyright
PROCESS FOR THE PREPARATION OF IODIDES
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Page/Page column 28-30, (2012/01/05)
This invention is directed to a process for the preparation of high yield alkyl or aryl iodide from its corresponding carboxylic acid using N-iodo amides.
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