5896-17-3 | 2-Benzyloxybenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$10.00	$7.00
100g	98%	in stock	$17.00	$12.00
500g	98%	in stock	$84.00	$59.00

Description

• Catalog Number: AB61273
• Chemical Name: 2-Benzyloxybenzaldehyde
• CAS Number: 5896-17-3
• Molecular Formula: C14H12O2
• Molecular Weight: 212.24388000000002
• MDL Number: MFCD00016583
• SMILES: O=Cc1ccccc1OCc1ccccc1
• NSC Number: 401884

Computed Properties

• Complexity: 209
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• XLogP3: 3.2

Literature

• Copper(II) and nickel(II) complexes of benzyloxybenzaldehyde-4-phenyl-3-thiosemicarbazone: Synthesis, characterization and biological activity.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20100915

• (E)-N'-(2-Benzyl-oxybenzyl-idene)isonicotinohydrazide methanol solvate monohydrate.

  Acta crystallographica. Section E, Structure reports online 20100601

• Phosphorylation State-Dependent High Throughput Screening of the c-Met Kinase.

  Current chemical genomics 20100101

• Synthesis and evaluation of pyrido[1,2-a]pyrimidines as inhibitors of nitric oxide synthases.

  European journal of medicinal chemistry 20090701

• Total synthesis of three naturally occurring 6,8-di-C-glycosylflavonoids: phloretin, naringenin, and apigenin bis-C-beta-D-glucosides.

  Carbohydrate research 20060612

• Synthesis of (2E)-3-{2-[(substituted benzyl)oxy]phenyl}acrylaldehydes as novel anti-inflammatory agents.

  Bioorganic & medicinal chemistry letters 20060515

• Synthesis and anticancer activity of benzyloxybenzaldehyde derivatives against HL-60 cells.

  Bioorganic & medicinal chemistry 20050301

• 2-Benzyloxybenzaldehyde inhibits formyl peptide-stimulated increase in intracellular Ca2+ in neutrophils mainly by blocking Ca2+ entry.

  Naunyn-Schmiedeberg's archives of pharmacology 20041101

• Investigation of the cellular mechanism of inhibition of formyl-methionyl-leucyl-phenylalanine-induced superoxide anion generation in rat neutrophils by 2-benzyloxybenzaldehyde.

  Biochemical pharmacology 20030401

• 2-Benzyloxybenzaldehyde inhibits formyl-methionyl-leucyl-phenylalanine stimulation of phospholipase D activation in rat neutrophils.

  Biochimica et biophysica acta 20021010

• Inhibition of Ras-mediated cell proliferation by benzyloxybenzaldehyde.

  Journal of biomedical science 20020101

• Benzyloxybenzaldehyde analogues as novel adenylyl cyclase activators.

  Bioorganic & medicinal chemistry letters 20010806