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
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 |
