941-98-0 | 1'-Acetonaphthone

Packsize	Purity	Availability	Price	Discounted Price
100g	98%	in stock	$13.00	$9.00
500g	98%	in stock	$43.00	$30.00
1000g	98%	in stock	$86.00	$60.00

Description

• Catalog Number: AB43230
• Chemical Name: 1'-Acetonaphthone
• CAS Number: 941-98-0
• Molecular Formula: C12H10O
• Molecular Weight: 170.2072
• MDL Number: MFCD00004013
• SMILES: CC(=O)c1cccc2c1cccc2
• NSC Number: 7659

Computed Properties

• Complexity: 197
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.9

Literature

• Modulation of photophysics and photodynamics of 1'-hydroxy-2'-acetonaphthone (HAN) in bile salt aggregates: a study of polarity and nanoconfinement effects.

  The journal of physical chemistry. B 20120802

• Asymmetric reduction of a ketone by wet and lyophilized cells of Geotrichum candidum in organic solvents.

  New biotechnology 20120215

• (E)-1-(Naphthalen-1-yl)-3-(1-phenyl-1H-pyrazol-4-yl)prop-2-en-1-one.

  Acta crystallographica. Section E, Structure reports online 20111001

• trans-Chlorido(phenanthren-9-yl)bis-(triphenyl-phosphane)nickel(II).

  Acta crystallographica. Section E, Structure reports online 20110901

• 2-Amino-6-(naphthalen-1-yl)-4-phenyl-pyridine-3-carbonitrile.

  Acta crystallographica. Section E, Structure reports online 20110401

• Chemistry of the enaminone of 1-acetylnaphthalene under microwave irradiation using chitosan as a green catalyst.

  Molecules (Basel, Switzerland) 20110117

• Screening for estrogenic and antiestrogenic activities of plants growing in Egypt and Thailand.

  Pharmacognosy research 20110101

• (2E)-3-(2-Chloro-6-methyl-3-quinol-yl)-1-(1-naphth-yl)prop-2-en-1-one.

  Acta crystallographica. Section E, Structure reports online 20100401

• (E)-3-(4-Chloro-phen-yl)-1-(1-naphth-yl)prop-2-en-1-one.

  Acta crystallographica. Section E, Structure reports online 20091201

• Synthesis and antihyperglycemic activity of 2-(substituted phenyl)-3-{[4-(1-naphthyl)-1,3-thiazol-2-yl] amino}-4-oxo-1,3-thiazolidin-5-ylacetic acid derivatives.

  Acta poloniae pharmaceutica 20090101

• Toxicity, tunneling and feeding behavior of the termite, Coptotermes vastator, in sand treated with oil of the physic nut, Jatropha curcas.

  Journal of insect science (Online) 20090101

• Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.

  Chemical research in toxicology 20080401

• Improvement of carbonyl reductase production of Geotrichum candidum for the transformation of 1-acetonaphthone to S(-)-1-(1'-napthyl) ethanol.

  Bioresource technology 20070701

• A ruthenium-catalyzed reaction of aromatic ketones with arylboronates: a new method for the arylation of aromatic compounds via C-H bond cleavage.

  Journal of the American Chemical Society 20030219