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  2. 1,9-Decadiene, 3,3,4,4,5,5,6,6,7,7,8,8-dodecafluoro-

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,9-Decadiene, 3,3,4,4,5,5,6,6,7,7,8,8-dodecafluoro-

C=CC(C(C(C(C(C(C=C)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F Request for Quotation
Chemical Name: 1,9-Decadiene, 3,3,4,4,5,5,6,6,7,7,8,8-dodecafluoro-
CAS Number: 1800-91-5
Product Number: AG0021LC(AGN-PC-0JLD3W)
Synonyms:
MDL No:
Molecular Formula: C10H6F12
Molecular Weight: 354.1355

Identification/Properties

Computed Properties
Molecular Weight:
354.139g/mol
XLogP3:
5.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
12
Rotatable Bond Count:
7
Exact Mass:
354.028g/mol
Monoisotopic Mass:
354.028g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
405
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,6-Divinylperfluorohexane, a unique and versatile compound, finds widespread applications in chemical synthesis as a valuable building block. Due to its fluorinated structure, this compound plays a crucial role in creating complex molecular structures with enhanced properties. In chemical synthesis, 1,6-Divinylperfluorohexane acts as a key component in the production of specialty polymers, surfactants, and materials with tailored functionalities. Its ability to undergo various types of reactions and form strong covalent bonds enables it to be utilized in the development of advanced materials and innovative chemical processes. Additionally, the perfluorinated nature of 1,6-Divinylperfluorohexane imparts exceptional chemical and thermal stability to the final products, making it an indispensable ingredient in the realm of chemical synthesis.