TargetMol

Perfluoro(1,3-dimethylcyclohexane)

Product Code:
 
TAR-T21075
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20°C
1 / 1

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Further Information

Bioactivity:
Perfluoro-1,3-dimethylcyclohexane is used as a synthesis reagent for amorphous fluorocarbon film preparation by plasma polymerization, and for the hydroformylation of linear terminal alkenes. As a chemically inert compound, it is similar in properties to other perfluorocarbons.
CAS:
335-27-3
Molecular Weight:
400.06
Purity:
0.98
SMILES:
FC(F)(F)C1(F)C(F)(F)C(F)(F)C(F)(F)C(F)(C(F)(F)F)C1(F)F

References

Rauh F, Schwenk M, Pejcic B, Myers M, Ho KB, Stalker L, Mizaikoff B. A mid-infrared sensor for the determination of perfluorocarbon-based compounds in aquatic systems for geosequestration purposes. Talanta. 2014 Dec;130:527-35. doi: 10.1016/j.talanta.2014.07.025. Epub 2014 Jul 25. PubMed PMID: 25159442. Westbrook AW, Ren X, Moo-Young M, Chou CP. Application of hydrocarbon and perfluorocarbon oxygen vectors to enhance heterologous production of hyaluronic acid in engineered Bacillus subtilis. Biotechnol Bioeng. 2018 May;115(5):1239-1252. doi: 10.1002/bit.26551. Epub 2018 Feb 26. PubMed PMID: 29384194. Pozzi G, Fish RH. Fluoroponytailed crown ethers and quaternary ammonium salts as solid-liquid phase transfer catalysts in organic synthesis. Top Curr Chem. 2012;308:213-32. doi: 10.1007/128_2011_240. PubMed PMID: 21928010. Wenska G, Taras-Go?li?ska K, ?ukaszewicz A, Burdzi?ski G, Koput J, Maciejewski A. Mechanism and dynamics of intramolecular triplet state decay of 1-propyl-4-thiouracil and its ?-methyl-substituted derivatives studied in perfluoro-1,3-dimethylcyclohexane. Photochem Photobiol Sci. 2011 Aug;10(8):1294-302. doi: 10.1039/c1pp05034f. Epub 2011 May 19. PubMed PMID: 21594285.