Perfluoro(2-methyl-2-pentene)

Name: Perfluoro(2-methyl-2-pentene)
SKU: ACM1584038
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Catalog NumberACM1584038

CAS Number1584-03-8

CategoryPolymers

IUPAC Name

1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pent-2-ene

Molecular Weight

300.04g/mol

Molecular Formula

C6F12

Canonical SMILES

C(=C(C(C(F)(F)F)(F)F)F)(C(F)(F)F)C(F)(F)F

InChI

InChI=1S/C6F12/c7-2(3(8,9)6(16,17)18)1(4(10,11)12)5(13,14)15

InChI Key

FAEGGADNHFKDQX-UHFFFAOYSA-N

Application

Perfluoro(2-methyl-2-pentene) serves crucial roles in various chemical processes and industrial applications. As a versatile compound, it acts as a key ingredient in fabricating waterproof and oilproof Si/F-modified polyurethane finishing agents for textiles and leather. Additionally, it contributes to the production of polyurethane foams by functioning as a blowing agent. In the realm of chemical reactions, Perfluoro(2-methyl-2-pentene) engages with α-oxides in the presence of cesium fluoride (CsF) to form olefins that incorporate the perfluoro(dimethylpropyl)methyl group and cesium perfluoro-2-methyl-penten-3-olate. Furthermore, when it interacts with epichlorohydrin alongside CSP, it yields a range of complex fluorinated compounds, including trans-1,1,1,7,7,8,8,9,9,9-decafluoro-2,6,6-tris(trifluoromethyl)-4-nonene. Under the influence of CsF, it partially converts to a more stable hexafluoropropylene trimer, perfluoro-2,4-dimethyl-3-heptene, showcasing its adaptability in synthesis. When reacted with alcohols, it can produce fluorine substitution or addition products, depending on the catalyst level, and with branched alcohols, it may also form isomeric vinyl ethers, diversifying its chemical utility.

Complexity

319

Covalently-Bonded Unit Count

EC Number

216-436-1

Exact Mass

299.980838g/mol

Formal Charge

Heavy Atom Count

MeSH Entry Terms

perfluoro-2-methyl-2-pentene

Monoisotopic Mass