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
Canonical 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 ℃
Flash Point
14 ℃
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.
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)
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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