Pentafluorophenylmethacrylate

Product Information

Molecular Formula:
C10H5F5O2
Molecular Weight:
252.14
Description
Applications: Pentafluorophenyl methacrylate is a useful research chemical.
Synonyms
PENTAFLUOROPHENYL METHACRYLATE
IUPAC Name
(2,3,4,5,6-pentafluorophenyl) 2-methylprop-2-enoate
Canonical SMILES
CC(=C)C(=O)OC1=C(C(=C(C(=C1F)F)F)F)F
InChI
InChI=1S/C10H5F5O2/c1-3(2)10(16)17-9-7(14)5(12)4(11)6(13)8(9)15/h1H2,2H3
InChI Key
NIJWSVFNELSKMF-UHFFFAOYSA-N
Flash Point
77 °C
Purity
>97.0%(GC)
Density
1.41
Appearance
Colorless to Light yellow to Light orange clear liquid
Storage
0-10°C
Refractive Index
1.44

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].

Computed Properties

XLogP3
3.1
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
7
Rotatable Bond Count
3
Exact Mass
252.02097021 g/mol
Monoisotopic Mass
252.02097021 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
17
Formal Charge
0
Complexity
306
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-113999354-A Amphiphilic block polymer nanoparticles with different morphologies and preparation method and application thereof 2021-12-07
CN-112807433-A Green light response polymer nano-drug carrier and preparation method thereof 2021-02-19
CN-112807433-B Green light response macromolecule nano-drug carrier 2021-02-19
CN-112759728-A TEMPO-containing reduction-responsive amphiphilic core cross-linked polymer, polymer drug-loaded micelle and preparation method thereof 2020-12-30
CN-112709068-A Composite material for petrochemical wastewater treatment and preparation method thereof 2020-12-29
CN-112326857-A Detection method of perfluorinated compounds 2020-10-22
JP-2022029023-A Creation of functional composite fine particles using a gradient type polymer surfactant and a liquid drying method in combination 2020-08-04
JP-2022029024-A Creation of functional composite fine particles using a combination of an end-mixed block-type polymer surfactant and an in-liquid drying method 2020-08-04
JP-2022029025-A Creation of functional composite fine particles using a polymer surfactant synthesized by precision polymerization and an in-liquid drying method in combination. 2020-08-04
CN-111704704-A Ultrahigh-resolution anti-etching metal-containing block copolymer, and preparation and application thereof 2020-06-04

Literatures

PMID Publication Date Title Journal
22714316 2012-06-04 Low loss graded index polymer optical fiber with high stability under damp heat conditions Optics express
22381078 2012-03-27 Cationic nanohydrogel particles as potential siRNA carriers for cellular delivery ACS nano
21732702 2011-08-08 Side-chain peptide-synthetic polymer conjugates via tandem 'ester-amide/thiol-ene' post-polymerization modification of poly(pentafluorophenyl methacrylate) obtained using ATRP Biomacromolecules
21143997 2010-12-12 Nanometric self-assembling peptide layers maintain adult hepatocyte phenotype in sandwich cultures Journal of nanobiotechnology
20831201 2010-10-11 Immobilization of biomolecules to plasma polymerized pentafluorophenyl methacrylate Biomacromolecules
21567557 2010-09-01 Synthesis, Characterization and Preliminary Biological Evaluation of P(HPMA)-b-P(LLA) Copolymers: A New Type of Functional Biocompatible Block Copolymer Macromolecular rapid communications
17338554 2007-03-27 Surface reactivity of pulsed-plasma polymerized pentafluorophenyl methacrylate (PFM) toward amines and proteins in solution Langmuir : the ACS journal of surfaces and colloids
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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