Home Aldehydes 2-Benzyloxybenzaldehyde

2-Benzyloxybenzaldehyde

CAS No.:
5896-17-3
Catalog Number:
AG003GLD
Molecular Formula:
C14H12O2
Molecular Weight:
212.2439
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$19
- +
25g
98%
In Stock USA
United States
$38
- +
100g
98%
In Stock USA
United States
$100
- +
500g
98%
In Stock USA
United States
$282
- +
Product Description
Catalog Number:
AG003GLD
Chemical Name:
2-Benzyloxybenzaldehyde
CAS Number:
5896-17-3
Molecular Formula:
C14H12O2
Molecular Weight:
212.2439
MDL Number:
MFCD00016583
IUPAC Name:
2-phenylmethoxybenzaldehyde
InChI:
InChI=1S/C14H12O2/c15-10-13-8-4-5-9-14(13)16-11-12-6-2-1-3-7-12/h1-10H,11H2
InChI Key:
PBEJTRAJWCNHRS-UHFFFAOYSA-N
SMILES:
O=Cc1ccccc1OCc1ccccc1
EC Number:
611-766-6
NSC Number:
401884
Properties
Complexity:
209  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
212.084g/mol
Formal Charge:
0
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
212.248g/mol
Monoisotopic Mass:
212.084g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.2  
Literature
Title Journal
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
Properties