1,1,1,3,3,3-Hexafluoroisopropyl acrylate
Product Information
Molecular Formula
C6H4F6O2
Molecular Weight
222.09
Description
Applications: 1,1,1,3,3,3-Hexafluoroisopropyl acrylate is a useful research chemical.
Synonyms
1,1,1,3,3,3-hexafluoropropan-2-yl prop-2-enoate
IUPAC Name
1,1,1,3,3,3-hexafluoropropan-2-yl prop-2-enoate
SMILES
C=CC(=O)OC(C(F)(F)F)C(F)(F)F
InChI
InChI=1S/C6H4F6O2/c1-2-3(13)14-4(5(7,8)9)6(10,11)12/h2,4H,1H2
InChI Key
MNSWITGNWZSAMC-UHFFFAOYSA-N
Boiling Point
84 °C
Flash Point
14 °C
Purity
95 %
Density
1.33 g/cm3
Appearance
Clear colorless liquid
Storage
Flammables area
Refractive Index
1.32
LogP
2.20880
Safety Information
Hazards
H225:
Highly flammable liquid and vapour.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
H411:
Toxic to aquatic life with long-lasting effects.
Highly flammable liquid and vapour.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
H411:
Toxic to aquatic life with long-lasting effects.
Precautionary Statement
P210, P233, P240, P241, P242, P243, P261, P264, P271, P273, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P391, P403+P233, P403+P235, P405, and P501
Signal Word
Danger
Computed Properties
XLogP3
3
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
8
Rotatable Bond Count
3
Exact Mass
222.01154834 g/mol
Monoisotopic Mass
222.01154834 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
214
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-114058198-A | Composition for packaging OLED, packaging film layer and OLED display | 2022-01-07 |
| CN-114149796-A | Double-hydrophobic fluorine-containing nano fluid and preparation method and application thereof | 2021-11-10 |
| CN-113451561-A | Silicon-based composite material and preparation method and application thereof | 2021-08-30 |
| CN-113451561-B | Silicon-based composite material and preparation method and application thereof | 2021-08-30 |
| CN-113675471-A | Battery electrolyte and battery comprising same | 2021-08-12 |
| CN-113675473-A | Electrolyte and battery containing same | 2021-08-12 |
| CN-113593408-A | Display module, manufacturing method thereof and mobile terminal | 2021-07-07 |
| CN-113150022-A | 3-substituted five-membered cyclic borate derivative, and pharmaceutical composition and pharmaceutical application thereof | 2021-04-23 |
| CN-113214302-A | 3-substituted five-membered cyclic borate derivative for inhibiting metal beta-lactamase and/or serine beta-lactamase | 2021-04-23 |
| CN-112876688-A | Preparation method of nano micelle suitable for tandem catalysis | 2021-01-20 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 21043506 | 2010-11-24 | Mechanical activation of catalysts for C-C bond forming and anionic polymerization reactions from a single macromolecular reagent | Journal of the American Chemical Society |
| 20827030 | 2010-10-01 | Kinetic polymerization behavior of fluorinated monomers for dental use | Dental materials journal |
| 19787137 | 2009-10-21 | Enantio- and stereoselective route to the phoslactomycin family of antibiotics: formal synthesis of (+)-fostriecin and (+)-phoslactomycin B | Chemical communications (Cambridge, England) |
| 17078717 | 2006-11-09 | Beta-isocupreidine-catalyzed Baylis-Hillman reaction of chiral N-boc-alpha-amino aldehydes | Organic letters |
| 12916992 | 2003-08-21 | beta-Isocupreidine-catalyzed asymmetric Baylis-Hillman reaction of imines | Organic letters |
| 12240274 | 2001-10-07 | An enantio- and stereocontrolled synthesis of (-)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis-Hillman reaction | Chemical communications (Cambridge, England) |
