CAS 6315-96-4

1-(2-Naphthalenyl)-1-propanone

Description:

1-(2-Naphthalenyl)-1-propanone, also known as 2-Naphthylacetone, is an organic compound characterized by its structure, which features a naphthalene ring attached to a propanone group. This compound typically appears as a pale yellow to light brown liquid or solid, depending on its purity and temperature. It has a distinct aromatic odor, indicative of its naphthalene component. The molecular formula of 1-(2-Naphthalenyl)-1-propanone reflects its composition, which includes carbon, hydrogen, and oxygen atoms. It is known for its applications in organic synthesis, particularly in the production of various pharmaceuticals and fragrances. The compound exhibits moderate solubility in organic solvents, while being less soluble in water due to its hydrophobic nature. Additionally, it may undergo typical organic reactions such as oxidation and reduction, making it a versatile intermediate in chemical synthesis. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure.

Formula: C₁₃H₁₂O

InChI: InChI=1S/C13H12O/c1-2-13(14)12-8-7-10-5-3-4-6-11(10)9-12/h3-9H,2H2,1H3

InChI key: InChIKey=QLYPHTMKMPIJNG-UHFFFAOYSA-N

SMILES: C(CC)(=O)C1=CC2=C(C=C1)C=CC=C2

Synonyms:

• 1-(2-Naphthalenyl)-1-propanone
• 1-(2-Naphthyl)-1-propanone
• 1-(Naphthalen-2-Yl)Propan-1-One
• 1-Propanone, 1-(2-naphthalenyl)-
• 2-Propionaphthone
• 2-Propionylnaphthalene
• NSC 21044
• β-Propionaphthone
• 1-(2-Naphthyl)propan-1-one

1-(2-naphthyl)propan-1-one

CAS: 6315-96-4

Formula: C₁₃H₁₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 184.2338

Ref: IN-DA00EJZA

1-(Naphthalen-2-yl)propan-1-one

CAS: 6315-96-4

1-(Naphthalen-2-yl)propan-1-one

Purity: 97%

Molecular weight: 184.24g/mol

Ref: 54-OR1057530

1-Naphthalen-2-yl-propan-1-one

CAS: 6315-96-4

Purity: 97%

Molecular weight: 184.2380066

Ref: 10-F735512

1-naphthalen-2-ylpropan-1-one

CAS: 6315-96-4

1-naphthalen-2-ylpropan-1-one is a linear acyl compound that is used in the synthesis of other compounds. It reacts with propanoic acid to form 1,2-diphenylethane. The reaction also produces an acylation product and propanoic acid as a byproduct. This reaction is an example of an acylation reaction, which is the process of adding an organic acid group to a hydrocarbon molecule. The result of this reaction is shown in the diagram below.

Formula: C₁₃H₁₂O

Purity: Min. 95%

Molecular weight: 184.23 g/mol

Ref: 3D-GAA31596