107650-06-6 Usage
General Description
1H,1H,2H,3H,3H-Perfluorononane-1,2-diol is a complex organic compound known for its utility across a variety of industrial applications. This chemical is characterized by its long carbon chain, which is fully fluorinated, and its two hydroxyl groups at one end. Its unique molecular structure makes it highly stable and resistant to harsh conditions, making it an ideal ingredient in lubricants, surfactants, or other products requiring extreme thermal or chemical stability. However, due to the pervasive nature of perfluorinated compounds in the environment and their potential toxicity, there has been increased scrutiny on their use.
Check Digit Verification of cas no
The CAS Registry Mumber 107650-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107650-06:
(8*1)+(7*0)+(6*7)+(5*6)+(4*5)+(3*0)+(2*0)+(1*6)=106
106 % 10 = 6
So 107650-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F13O2/c10-4(11,1-3(24)2-23)5(12,13)6(14,15)7(16,17)8(18,19)9(20,21)22/h3,23-24H,1-2H2
107650-06-6Relevant articles and documents
Synthesis and characterization of perfluorohexylated poly(3,4-ethylenedioxythiophene)
Zuo, Liangbin,Qing, Feng-Ling,Meng, Wei-Dong,Huang, Xiaoyu,Zhang, Sen,Wu, Qiang
, p. 1441 - 1446 (2007/10/03)
The perfluorohexylated 3,4-ethylenedioxythiophene 5 was prepared via Mitsunobu reaction of perfluorohexylatyed diol 2 with diethyl 3,4-dihydroxythiophenedicarboxylate followed by decarboxylation. The polymerization of 5 was conducted with both oxidative chemical and electrochemical polymerizations. The polymers were characterized by cyclic voltammogram, UV, IR, TGA and DSC.
