Home Aldehydes 5896-17-3
5896-17-3,MFCD00016583
Catalog No.:AA003GIL

5896-17-3 | 2-Benzyloxybenzaldehyde

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5g
97%
in stock  
$6.00   $4.00
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10g
97%
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$7.00   $5.00
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25g
97%
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$12.00   $8.00
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100g
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500g
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$125.00   $88.00
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  • Technical Information
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003GIL
Chemical Name:
2-Benzyloxybenzaldehyde
CAS Number:
5896-17-3
Molecular Formula:
C14H12O2
Molecular Weight:
212.2439
MDL Number:
MFCD00016583
SMILES:
O=Cc1ccccc1OCc1ccccc1
NSC Number:
401884
Properties
Properties
 
BP:
326 °C at 760 mmHg  
Form:
Liquid  
MP:
46-47 °C  
Refractive Index:
n20/D 1.6(lit.)  
Stability:
Air Sensitive  
Storage:
Room Temperature;  

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

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

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20100915

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

Journal: Acta crystallographica. Section E, Structure reports online 20100601

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

Journal: Current chemical genomics 20100101

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

Journal: European journal of medicinal chemistry 20090701

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

Journal: Carbohydrate research 20060612

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

Journal: Bioorganic & medicinal chemistry letters 20060515

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

Journal: Bioorganic & medicinal chemistry 20050301

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

Journal: Naunyn-Schmiedeberg's archives of pharmacology 20041101

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

Journal: Biochemical pharmacology 20030401

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

Journal: Biochimica et biophysica acta 20021010

Title: Inhibition of Ras-mediated cell proliferation by benzyloxybenzaldehyde.

Journal: Journal of biomedical science 20020101

Title: Benzyloxybenzaldehyde analogues as novel adenylyl cyclase activators.

Journal: Bioorganic & medicinal chemistry letters 20010806

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