N-Phenylacrylamide

Product Information

Molecular Formula:
C9H9NO
Molecular Weight:
147.17
Description
N-Phenylacrylamide (CAS# 2210-24-4) is a useful research chemical.
Synonyms
N-phenyl-2-propenamide; N-phenylprop-2-enamide
IUPAC Name
N-phenylprop-2-enamide
Canonical SMILES
C=CC(=O)NC1=CC=CC=C1
InChI
InChI=1S/C9H9NO/c1-2-9(11)10-8-6-4-3-5-7-8/h2-7H,1H2,(H,10,11)
InChI Key
BPCNEKWROYSOLT-UHFFFAOYSA-N
Boiling Point
145-150 ℃ (Press: 3 Torr)
Melting Point
103-106 ℃ (lit.)
Purity
> 98.0 % (GC) (N)
Density
1.097±0.06 g/cm3(Predicted)
Appearance
White to almost white powder to crystal
LogP
1.88410

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
1.8
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
147.068413911 g/mol
Monoisotopic Mass
147.068413911 g/mol
Topological Polar Surface Area
29.1Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
148
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-114181682-A High-temperature-resistant salt-resistant cross-linked polymer filtrate reducer and preparation method and application thereof 2021-12-21
CN-114014858-A Process for preparing polysubstituted indolizine derivatives 2021-12-03
JP-2022024056-A Exterior material for power storage device and power storage device using it 2021-11-12
CN-113321765-A Double-liquid-phase acid liquid thickener and preparation method thereof 2021-08-03
CN-113321765-B Double-liquid-phase acid liquid thickener and preparation method thereof 2021-08-03
CN-113321766-A Multi-element association type fracturing fluid thickening agent and preparation method thereof 2021-08-03
CN-113321766-B Multi-element association type fracturing fluid thickening agent and preparation method thereof 2021-08-03
CN-113582946-A 3-aryl-5-thio-1, 3, 4-thiadiazole-2-thioketone derivative and preparation method and application thereof 2021-07-30
CN-113292573-A Indolizine chromogen ketone compound with anti-tumor activity and preparation method and application thereof 2021-06-09
CN-113325049-A Slightly-swelling biocompatible film and preparation method thereof 2021-04-29

Literatures

PMID Publication Date Title Journal
22705022 2012-07-15 Synthesis, biological evaluation and molecular docking studies of 3-(1,3-diphenyl-1H-pyrazol-4-yl)-N-phenylacrylamide derivatives as inhibitors of HDAC activity Bioorganic & medicinal chemistry
22224594 2012-02-09 Discovery and structure-activity relationship of potent and selective covalent inhibitors of transglutaminase 2 for Huntington's disease Journal of medicinal chemistry
22196975 2012-02-01 A comparative assessment of α-lipoic acid N-phenylamides as non-steroidal androgen receptor antagonists both on and off gold nanoparticles Bioorganic chemistry
22294093 2012-01-31 Competing pathways control host resistance to virus via tRNA modification and programmed ribosomal frameshifting Molecular systems biology
21469720 2011-05-05 Effects of dynamical couplings in IR spectra of the hydrogen bond in N-phenylacrylamide crystals The journal of physical chemistry. A
15064899 2004-04-01 Analysis of wheat extracts for ochratoxin A by molecularly imprinted solid-phase extraction and pulsed elution Analytical and bioanalytical chemistry
14715294 2004-02-01 Tris(2-carboxyethyl)phosphine stabilization of RNA: comparison with dithiothreitol for use with nucleic acid and thiophosphoryl chemistry Analytical biochemistry
12558441 2003-02-07 Enantioselective [6pi]-photocyclization reaction of an acrylanilide mediated by a chiral host. Interplay between enantioselective ring closure and enantioselective protonation The Journal of organic chemistry
5789 1976-04-01 Hyperoxia and red cell 2,3-diphosphoglycerate Toxicology and applied pharmacology
4477 1976-03-01 A kinetic concepto of lipid transport in ruminants Journal of dairy science
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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