306-98-9 Usage
Description
Perfluoro-1,2-dimethylcyclohexane is a synthetic, perfluorinated organic compound characterized by its unique chemical and physical properties. It is a colorless liquid with a low boiling point and high chemical stability. The molecule consists of a cyclohexane ring with two methyl groups replaced by perfluorinated counterparts, which imparts exceptional hydrophobicity and resistance to chemical reactions.
Uses
Used in Nanotechnology and Surface Engineering:
Perfluoro-1,2-dimethylcyclohexane is used as a processing fluid for the manufacturing of surface nanoprotrusion structures using a polymer stamp with colloidal particles. Its unique properties, such as low surface tension and high chemical inertness, make it an ideal candidate for this application, as it allows for the precise control and manipulation of colloidal particles during the nanoprotrusion process.
In the field of nanotechnology, the use of Perfluoro-1,2-dimethylcyclohexane enables the creation of intricate and highly detailed surface structures with potential applications in various industries, including electronics, materials science, and biotechnology. PERFLUORO-1,2-DIMETHYLCYCLOHEXANE's ability to facilitate the formation of these structures is due to its compatibility with a wide range of materials and its ability to provide a stable environment for the colloidal particles involved in the process.
Additionally, Perfluoro-1,2-dimethylcyclohexane's high chemical stability and resistance to degradation make it a valuable component in the development of long-lasting and durable nanostructures, which can withstand harsh environmental conditions and maintain their functionality over time. This characteristic is particularly important in applications where the integrity and performance of the nanostructures are critical, such as in the development of advanced sensors, energy storage devices, and medical implants.
Check Digit Verification of cas no
The CAS Registry Mumber 306-98-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 306-98:
(5*3)+(4*0)+(3*6)+(2*9)+(1*8)=59
59 % 10 = 9
So 306-98-9 is a valid CAS Registry Number.
InChI:InChI=1/C8F16/c9-1(7(19,20)21)2(10,8(22,23)24)4(13,14)6(17,18)5(15,16)3(1,11)12
306-98-9Relevant articles and documents
POLYFLUOROCYCLOALKENES. PART XIX. SOME REACTIONS AND COMPOUNDS FROM 1,2-BIS(TRIFLUOROMETHYL)OCTAFLUOROCYCLOHEXENE
Collins, David,Stephens, Robert,Tatlow, John Colin
, p. 213 - 228 (2007/10/02)
The title compound (A) gave a dichloro-adduct (D), which with lithium aluminum hydride yielded a complex mixture, from which a trace of trans 1H,2H-1,2-bis(trifluoromethyl)octafluorocyclohexane (E) was isolated.Catalytic hydrogenation of olefin (A) afforded cis 1H,2H-1,2-bis(trifluoromethyl)octafluorocyclohexane (C), and a small amount of 6H-1,6-bis(trifluoromethyl)heptafluorocyclohexene (B).Dehydrofluorination of the cis dihydride (C) by aqueous potash gave olefin (B) and 2,3-bis(trifluoromethyl)hexafluorocyclohexa-1,3-diene (G): fluorination of (G) by cobalt(III) fluoride gave back (A).Fluorination of compounds (C) and (B) afforded cis and trans 1H-1,2-bis(trifluoromethyl)nonafluorocyclohexane (J and H respectively).Both (H) and (J) were dehydrofluorinated to give olefin (A) exclusively, i.e. fluorine was lost preferentially from the tertiary ->C-F group.Ammonia and (A) gave 1,3-diamino-2-cyano-3-trifluoromethylhexafluorocyclohexene (K).Some hydro-polyfluoro-cyclohexanes took up small proportions of deuterium during dehydrofluorinations in the presence of deuterium oxide,but no interconversions of pairs of stereoisomers were observed.
