2,2,3,3,4,4,5,5-Octafluoro-1,6-hexanediol

Product Information

Molecular Formula:
C6H6F8O2
Molecular Weight:
262.0979
Description
2,2,3,3,4,4,5,5-Octafluoro-1,6-hexanediol is a complex fluorine-labeled component that is deeply integrated into the pharmaceutical process. It exhibits profound fluorine clustering and is capable of significant interactions with protein entities.
Synonyms
1,6-Hexanediol, 2,2,3,3,4,4,5,5-octafluoro-; 1,6-DIHYDROXY-2,2,3,3,4,4,5,5-OCTAFLUOROHEXANE; 2,2,3,3,4,4,5,5-OCTAFLUORO-1,6-HEXANEDIOL; 2,2,3,3,4,4,5,5-OCTAFLUOROHEXAN-1,6-DIOL; 2,2,3,3,4,4,5,5-OCTAFLUOROHEXANE-1,6-DIOL; 1H,1H,6H,6H-OCTAFLUOROHEXANE-1,6-DIOL
IUPAC Name
2,2,3,3,4,4,5,5-octafluorohexane-1,6-diol
Canonical SMILES
C(C(C(C(C(CO)(F)F)(F)F)(F)F)(F)F)O
InChI
InChI=1S/C6H6F8O2/c7-3(8,1-15)5(11,12)6(13,14)4(9,10)2-16/h15-16H,1-2H2
InChI Key
NHEKBXPLFJSSBZ-UHFFFAOYSA-N
Boiling Point
262.4°C at 760 mmHg 100°C3 mm Hg(lit.)
Melting Point
66-70°C(lit.)
Flash Point
100°C/3mm
Purity
98.0%
Density
1.575 g/cm3
Appearance
white to off-white crystalline solid

Computed Properties

XLogP3
1.5
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
10
Rotatable Bond Count
5
Exact Mass
262.02400473 g/mol
Monoisotopic Mass
262.02400473 g/mol
Topological Polar Surface Area
40.5Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
225
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

Patents

Publication Number Title Priority Date
CN-114043914-A Automobile carpet with composite fiber structure and preparation method thereof 2021-11-29
CN-112851906-A Preparation method of fluorine-containing isocyanate type curing agent 2021-01-14
CN-111848995-A Manufacturing method of quantum dot film with high water vapor isolation 2020-07-20
CN-111748279-A High-weather-resistance stain-resistant coating composition based on fluorine-containing diol and polysiloxane copolymerization modified polyester and preparation method thereof 2020-07-10
CN-111748279-B High-weather-resistance stain-resistant coating composition based on fluorine-containing diol and polysiloxane copolymerization modified polyester and preparation method thereof 2020-07-10
WO-2021230214-A1 Organic electroluminescence element, manufacturing method thereof, simple display device equipped with same, and printed matter 2020-05-13
CN-113204170-A Resist underlayer composition and method for forming pattern using the same 2020-01-31
JP-2021124726-A Composition for resist underlayer film and pattern formation method using it 2020-01-31
US-2021240082-A1 Resist underlayer composition, and method of forming patterns using the composition 2020-01-31
TW-202130695-A Resist underlayer composition, and method of forming patterns using the composition 2020-01-31

Literatures

PMID Publication Date Title Journal
21192649 2011-01-27 Miscibility and multilayer formation of fluoroalkane-α,ω-diol mixtures at the air/water interface The journal of physical chemistry. B
19333452 2009-01-01 Strategy for adapting wine yeasts for bioethanol production International journal of molecular sciences
16771343 2006-06-08 Alpha-helix formation in melittin and beta-lactoglobulin A induced by fluorinated dialcohols The journal of physical chemistry. B
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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