63703-16-2 Usage
General Description
6H-Perfluorohexyl iodide is a chemical compound with the molecular formula C6F13I. It is classified as a perfluoroalkyl iodide, which is a group of chemicals characterized by a carbon chain fully substituted with fluorine atoms and a single iodine atom. 6H-Perfluorohexyl iodide is used as a starting material in organic synthesis, particularly in the preparation of fluorinated compounds. It is highly reactive due to the presence of the iodine atom, and its chemical properties make it useful in the production of various fluorinated materials for industrial and research purposes. Additionally, it is known for its water-repellent and low surface energy properties, making it potentially useful in applications such as water and oil repellent coatings. Overall, 6H-Perfluorohexyl iodide is a versatile chemical with a variety of applications in the field of organic chemistry and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 63703-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,0 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63703-16:
(7*6)+(6*3)+(5*7)+(4*0)+(3*3)+(2*1)+(1*6)=112
112 % 10 = 2
So 63703-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C6HF12I/c7-1(8)2(9,10)3(11,12)4(13,14)5(15,16)6(17,18)19/h1H
63703-16-2Relevant articles and documents
Complexation and Photoinduced Electron-transfer Reaction between Perfluoroalkyl Iodides and N,N,N',N'-Tetramethylphenylene-1,4-diamine, Anilines and Piperazines
Chen, Qing-Yun,Li, Zhan-Ting,Zhou, Cheng-Min
, p. 2457 - 2462 (2007/10/02)
Treatment of tetrafluoro-1,2-diiodoethane 1a or dodecafluoro-1,6-diiodohexane 1b with N,N,N',N'-tetramethylphenylene-1,4-diamine 2 gave 1 + 1 solid complexes 3a or 3b in high yields.Complex 3a decomposed to give tetrafluoroethylene, iodine and 2 when irradiated with UV or heated.Complex 3b was converted into 6H-dodecafluorohexyl-N,N,N',N'-tetramethylphenylene-1,4-diamine 4 when irradiated with UV.On treatment of 1a and 1b with piperazine 6a and N,N'-dimethylpiperazine 6b, 1 + 1 solid complexes 7 were similarly obtained.However, heating or irradiating 7 gave no perfluoroalkylated products.Irradiating a mixture of 2 or anilines 13 and perfluoroalkyl iodides 10 in dimethylformamide also gave perfluoroalkylated products.The photoinduced electron transfer reaction involved radical cation 2*+ as a reactive intermediate which was detected by EPR techniques.