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2'-Acetonaphthone

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Identification
Molecular formula
C13H10O
CAS number
941-98-0
IUPAC name
1-(2-naphthyl)prop-2-en-1-one
State
State

At room temperature, 2'-Acetonaphthone is in a solid state. Its crystalline structure and pale yellow color make it easily identifiable among other organic compounds used in similar applications. It is stable under normal conditions and typically undergoes sublimation at elevated temperatures.

Melting point (Celsius)
69.00
Melting point (Kelvin)
342.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
184.22g/mol
Molar mass
184.2210g/mol
Density
1.1360g/cm3
Appearence

2'-Acetonaphthone typically appears as a pale yellow crystalline solid. It possesses a characteristic aromatic odor, oftentimes used in perfumes to impart naphthalene or woody notes due to its naphthyl structure.

Comment on solubility

Solubility of 1-(2-naphthyl)prop-2-en-1-one (C13H10O)

1-(2-naphthyl)prop-2-en-1-one, also known as β-naphthylacrolein, exhibits intriguing solubility characteristics that can be summarized as follows:

  • Solvent Interaction: Generally soluble in organic solvents such as ethanol, acetone, and chloroform.
  • Poor Water Solubility: This compound shows limited solubility in water, which is typical for many organic compounds due to their hydrophobic nature.
  • Influence of Temperature: Solubility in organic solvents may increase with temperature, enhancing the solvation process.

Overall, the solubility properties of 1-(2-naphthyl)prop-2-en-1-one highlight its compatibility with non-polar and polar organic solvents, while remaining relatively insoluble in polar aqueous environments. This behavior is crucial for applications in organic synthesis and chemical formulations, making it an intriguing compound in various scientific studies.

Interesting facts

Interesting Facts about 1-(2-naphthyl)prop-2-en-1-one

1-(2-naphthyl)prop-2-en-1-one, also known as 2-naphthyl 1-acetylpropene, is a fascinating compound with a variety of applications in both organic chemistry and material science. Here are some engaging insights about this compound:

  • Structure and Reactivity: The compound features a unique conjugated structure with both a naphthyl group and an α,β-unsaturated carbonyl system. This structural feature makes it particularly reactive in electrophilic addition reactions and Michael additions.
  • Applications in Organic Synthesis: Due to its reactivity, 1-(2-naphthyl)prop-2-en-1-one is often used as a building block in organic synthesis for creating more complex molecules. Its ability to undergo various transformations is highly valued by chemists.
  • Fluorescent Properties: This compound exhibits interesting photophysical properties. When excited, it may show fluorescence, making it useful in fluorescence studies and applications like dye lasers.
  • Biological Relevance: Compounds similar to 1-(2-naphthyl)prop-2-en-1-one have shown potential biological activities, including anti-inflammatory and cancer-fighting properties, making it a candidate for pharmacological research.
  • Versatility: It has been studied for its potential use in the design of advanced materials, including polymers and organic light-emitting diodes, indicating its significance beyond traditional organic compounds.

As quoted by renowned chemist, “The beauty of chemistry lies in the ability to turn simple molecules into complex systems”. This sentiment rings true for 1-(2-naphthyl)prop-2-en-1-one, highlighting the endless possibilities this compound offers in the realm of chemical research.

Overall, 1-(2-naphthyl)prop-2-en-1-one stands as a remarkable compound with diverse applications and compelling properties, making it an exciting topic of study for scientists and students alike.

Synonyms
ZM 449829
4452-06-6
1-(naphthalen-2-yl)prop-2-en-1-one
1-naphthalen-2-ylprop-2-en-1-one
1-(2-Naphthalenyl)-2-propen-1-one
ZM449829
1-(2-naphthyl)prop-2-en-1-one
jak3 inhibitor v
JAK3-inhibitor-V
MFCD04974535
2-acryloylnaphthalene
Thr1 inhibitor, 1
2-naphthyl vinyl ketone
ZM-449829
BiomolKI_000064
BiomolKI2_000005
BMK1-G4
SCHEMBL149980
CHEMBL154580
SCHEMBL13158925
BDBM85122
CHEBI:93674
FOTCGZPFSUWZBN-UHFFFAOYSA-N
HMS3412I18
HMS3676I18
BCP07020
EX-A10475
HSCI1_000051
AKOS006293213
CCG-100668
JAK3 Inhibitor V - CAS 932258
NCGC00092279-01
NCGC00092279-02
NCGC00092279-03
BS-16843
HY-13450
DB-082069
CS-0006905
EN300-1843967
BRD-K95676198-001-02-6
BRD-K95676198-001-03-4
BRD-K95676198-001-05-9
Q27165369