93-08-3 | 2-Acetylnaphthalene

Packsize	Purity	Availability	Price	Discounted Price
25g	99%	in stock	$7.00	$5.00
100g	99%	in stock	$12.00	$9.00
500g	99%	in stock	$46.00	$33.00

Description

• Catalog Number: AI62208
• Chemical Name: 2-Acetylnaphthalene
• CAS Number: 93-08-3
• Molecular Formula: C12H10O
• Molecular Weight: 170.2072
• MDL Number: MFCD00004108
• SMILES: CC(=O)c1ccc2c(c1)cccc2
• NSC Number: 7658

Computed Properties

• Complexity: 197
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 3.2

Upstream Synthesis Route

1-(Naphthalen-2-yl)ethanone, also known as beta-naphthaldehyde, is a versatile compound widely utilized in chemical synthesis. This compound serves as a key building block in the creation of various organic molecules due to its unique structural properties. In chemical synthesis, 1-(Naphthalen-2-yl)ethanone is commonly employed as a precursor in the preparation of other organic compounds. Its reactive functionality enables it to participate in a variety of chemical reactions, such as Friedel-Crafts acylation, Grignard reactions, and Suzuki cross-coupling reactions. Incorporating 1-(Naphthalen-2-yl)ethanone into synthetic pathways allows for the efficient construction of complex molecules with diverse applications, ranging from pharmaceuticals and agrochemicals to materials science and liquid crystals. By leveraging the reactivity and structural characteristics of 1-(Naphthalen-2-yl)ethanone, chemists can access a broad array of chemical building blocks to enable the creation of novel and valuable compounds.

Literature

• Phenolic antioxidants inhibit the triplet-induced transformation of anilines and sulfonamide antibiotics in aqueous solution.

  Environmental science & technology 20120515

• Synthesis and characterization of privileged monodentate phosphoramidite ligands and chiral Brønsted acids derived from d-mannitol.

  International journal of molecular sciences 20120101

• Synthesis of biaryls via AlCl3 catalyzed domino reaction involving cyclization, dehydration, and oxidation.

  Organic letters 20111202

• Toxicity and inhibition of feeding and tunneling response of naphthalene and 10 derivatives on the formosan subterranean termite (Isoptera: Rhinotermitidae).

  Journal of economic entomology 20101201

• Synthesis, anticonvulsant and antimicrobial activities of some new 2-acetylnaphthalene derivatives.

  Bioorganic & medicinal chemistry 20100415

• 1-(2-Naphth-yl)-3-phenyl-prop-2-en-1-one.

  Acta crystallographica. Section E, Structure reports online 20090801

• Facile and efficient enantioselective Strecker reaction of ketimines by chiral sodium phosphate.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20090608

• Supra-nanosecond dynamics of a red-to-blue photon upconversion system.

  Inorganic chemistry 20090316

• [The triplet properties of beta-carotene in acetonitrile solution: a laser flash photolysis study].

  Guang pu xue yu guang pu fen xi = Guang pu 20080301

• On the effect of 1,4-diazabicyclo[2.2.2]octane on the singlet-oxygen dimol emission: photosensitized generation of (1O2)2.

  The journal of physical chemistry. A 20070524

• Aqueous oxidation of phenylurea herbicides by triplet aromatic ketones.

  Environmental science & technology 20061101

• Gas chromatography-microchip atmospheric pressure chemical ionization-mass spectrometry.

  Analytical chemistry 20060501

• Oxygen uptake and involvement of superoxide radicals upon photolysis of ketones in air-saturated aqueous alcohol, formate, amine or ascorbic acid solutions.

  Photochemistry and photobiology 20060101

• Binding properties of 2-acetylnaphthalene with hydroxypropyl cyclodextrins from fluorescence quenching experiments.

  Applied spectroscopy 20050501

• Environmental photodegradation of mefenamic acid.

  Chemosphere 20050301

• Rapid detection and characterization of minor reactive metabolites using stable-isotope trapping in combination with tandem mass spectrometry.

  Rapid communications in mass spectrometry : RCM 20050101

• Survivorship, tunneling and feeding behaviors of Coptotermes formosanus (Isoptera: Rhinotermitidae) in response to 2'-acetonaphthone-treated sand.

  Pest management science 20040801

• Probing the binding dynamics to sodium cholate aggregates using naphthalene derivatives as guests.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20031101

• Synthesis and anticonvulsant activity of some new dioxolane derivatives.

  Arzneimittel-Forschung 20030101