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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-Pentanol, 4,4,5,5,5-pentafluoro-

OCCCC(C(F)(F)F)(F)F Request for Quotation
Chemical Name: 1-Pentanol, 4,4,5,5,5-pentafluoro-
CAS Number: 148043-73-6
Product Number: AG001FDY(AGN-PC-0JSP9W)
Synonyms:
MDL No: MFCD00153224
Molecular Formula: C5H7F5O
Molecular Weight: 178.1005

Identification/Properties

Properties
BP:
73.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Refractive Index:
n20/D 1.33(lit.)
Computed Properties
Molecular Weight:
178.102g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
178.042g/mol
Monoisotopic Mass:
178.042g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H227-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,4,5,5,5-Pentafluoro-1-Pentanol is a highly versatile compound that serves as a valuable building block in various chemical synthesis processes. Due to its unique structural properties, this compound is commonly used as a reagent in the preparation of specialty chemicals, pharmaceuticals, and agrochemicals. Its strong electron-withdrawing nature and fluorinated structure make it particularly useful in reactions requiring strong acidic conditions or where enhanced stability and selectivity are desired. This compound can be employed as a key component in the synthesis of fluorinated organic molecules, which are of great interest in the field of medicinal chemistry and materials science. Additionally, 4,4,5,5,5-Pentafluoro-1-Pentanol plays a crucial role in the development of advanced polymers and surfactants, offering new opportunities for the design of high-performance materials with tailored properties.