Phenyl Acrylate

Product Information

Molecular Formula:
C9H8O2
Molecular Weight:
148.16
Description
UV absorbing monomer. Polymer n = ~1.55.
Synonyms
2-propenoic acid phenyl ester; phenyl prop-2-enoate
IUPAC Name
phenyl prop-2-enoate
Canonical SMILES
C=CC(=O)OC1=CC=CC=C1
InChI
InChI=1S/C9H8O2/c1-2-9(10)11-8-6-4-3-5-7-8/h2-7H,1H2
InChI Key
WRAQQYDMVSCOTE-UHFFFAOYSA-N
Boiling Point
98 °C / 24 mmHg
Flash Point
88 °C
Purity
> 98.0 % (GC)
Appearance
Colorless to light yellow clear liquid
Storage
Store at 4 degrees celsius
Refractive Index
n20/D 1.518
LogP
1.77800

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
H335:
May cause respiratory irritation.
H411:
Toxic to aquatic life with long-lasting effects.
Precautionary Statement
P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P391, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
2.1
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
3
Exact Mass
148.052429494 g/mol
Monoisotopic Mass
148.052429494 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
146
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
JP-2022040133-A A photosensitive coloring composition for a color filter for a solid-state image sensor, a color filter, and a solid-state image sensor using the same. 2021-12-15
CN-114149373-A 4-aryl substituted 2,4, 6-triene suberate and synthesis method thereof 2021-12-08
CN-114031339-A Phase change concrete and preparation method thereof 2021-11-25
CN-113912855-A Aziridine-based dispersant, preparation method and application thereof, and pigment slurry 2021-11-24
CN-113980654-A Graphene alloy composite phase change material and preparation method and application thereof 2021-11-18
CN-113897011-A Impact-resistant flexible protective material and preparation method thereof 2021-11-11
CN-113969091-A Water-based EVA (ethylene-vinyl acetate) treating agent and preparation method thereof 2021-11-03
JP-2022009139-A Radiation-sensitive resin composition 2021-10-14
CN-113651925-A Cool-feeling resin, photosensitive resin composition, and preparation method and application thereof 2021-09-24
CN-113801262-A High-strength gel and preparation method thereof 2021-09-18

Literatures

PMID Publication Date Title Journal
22719533 2012-06-01 Methyl (E)-2-[(2-nitro-phen-oxy)meth-yl]-3-phenyl-acrylate Acta crystallographica. Section E, Structure reports online
22259510 2012-01-01 (E)-Methyl 2-[(2-formyl-6-meth-oxy-phen-oxy)meth-yl]-3-phenyl-acrylate Acta crystallographica. Section E, Structure reports online
22199821 2011-12-01 (E)-Methyl 2-[(4-bromo-2-formyl-phen-oxy)meth-yl]-3-phenyl-acrylate Acta crystallographica. Section E, Structure reports online
17449047 2007-06-22 Influence of different polymerisation parameters on the separation efficiency of monolithic poly(phenyl acrylate-co-1,4-phenylene diacrylate) capillary columns Journal of chromatography. A
17328901 2007-04-13 Novel monolithic poly(phenyl acrylate-co-1,4-phenylene diacrylate) capillary columns for biopolymer chromatography Journal of chromatography. A
15771513 2005-03-23 Chiral phosphine lewis bases catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with activated olefins Journal of the American Chemical Society
15669042 2005-03-04 Catalytic, asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with activated olefins by quinidine-derived chiral amines Chemistry (Weinheim an der Bergstrasse, Germany)
15675792 2004-12-15 Antimicrobial activity of p-hydroxyphenyl acrylate derivatives Journal of agricultural and food chemistry
14725455 2004-01-23 Highly efficient aza-Baylis-Hillman reaction of N-tosylated imines with MVK, acrolein, and phenyl acrylate or alpha-naphthyl acrylate: Lewis base effects and a convenient method to synthesize alpha,beta-unsaturated beta-amino carbonyl compounds The Journal of organic chemistry
12809245 2003-06-07 Chiral phosphine Lewis base catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone and phenyl acrylate 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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