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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)-

Hexanoic acid, 4,4,5,5,6,6,6-heptafluoro-

OC(=O)CCC(C(C(F)(F)F)(F)F)(F)F Request for Quotation
Chemical Name: Hexanoic acid, 4,4,5,5,6,6,6-heptafluoro-
CAS Number: 356-02-5
Product Number: AG007A91(AGN-PC-0KKWHQ)
Synonyms:
MDL No:
Molecular Formula: C6H5F7O2
Molecular Weight: 242.0915

Identification/Properties

Computed Properties
Molecular Weight:
242.093g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
4
Exact Mass:
242.018g/mol
Monoisotopic Mass:
242.018g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
244
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1759
Hazard Statements:
H314
Precautionary Statements:
P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,4,5,5,6,6,6-Heptafluorohexanoic acid, commonly referred to as HFHA, serves as a versatile building block in chemical synthesis. This unique compound is utilized in various synthetic pathways to introduce fluorine atoms into organic molecules, offering enhanced stability, reactivity, and potentially beneficial properties.In organic synthesis, HFHA can act as a key intermediate in the preparation of fluorine-containing compounds, which are widely used in pharmaceuticals, agrochemicals, and materials science. Its highly reactive nature allows for selective fluorination reactions, providing a valuable tool for chemists to modify the properties of target molecules.Furthermore, HFHA can serve as a precursor for the synthesis of perfluorinated surfactants and polymers, due to its ability to impart hydrophobic and oleophobic characteristics to materials. This makes it an essential component in the manufacturing of anti-fouling coatings, water-repellent textiles, and other specialized products.Overall, the application of 4,4,5,5,6,6,6-Heptafluorohexanoic acid in chemical synthesis plays a crucial role in expanding the possibilities of molecular design and material engineering, contributing to advancements in various industries.