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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-Pentanamine,1,1,2,2,3,3,4,4,5,5,5-undecafluoro-N,N-bis(undecafluoropentyl)-

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Chemical Name: 1-Pentanamine,1,1,2,2,3,3,4,4,5,5,5-undecafluoro-N,N-bis(undecafluoropentyl)-
CAS Number: 338-84-1
Product Number: AG003V8O(AGN-PC-0R9DVL)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
-25
BP:
212-218 °C
Storage:
2-8℃;
Form:
Liquid
Refractive Index:
1.303
Computed Properties
Molecular Weight:
821.119g/mol
XLogP3:
11.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
34
Rotatable Bond Count:
12
Exact Mass:
820.95g/mol
Monoisotopic Mass:
820.95g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
49
Formal Charge:
0
Complexity:
1040
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


Tris(undecafluoropentyl)amine, also known as TUFPA, is a versatile and powerful compound used in various chemical synthesis processes. Its unique properties make it particularly valuable for a wide range of applications in the field of chemistry.In chemical synthesis, TUFPA serves as an effective catalyst for a number of reactions due to its strong nucleophilic nature. It can promote various transformations, such as cross-coupling reactions, nucleophilic additions, and metal-catalyzed processes. Additionally, TUFPA is known for its ability to activate substrates and facilitate the formation of challenging chemical bonds.Furthermore, TUFPA exhibits excellent solubility in a variety of organic solvents, making it easy to work with in different reaction conditions. Its stability and reactivity under a wide range of temperature and pressure conditions further enhance its utility in complex synthesis pathways.Overall, the application of Tris(undecafluoropentyl)amine in chemical synthesis offers chemists a valuable tool to accelerate and streamline the development of novel compounds and materials.