Home Aldehydes 4-Benzyloxybenzaldehyde

4-Benzyloxybenzaldehyde

CAS No.:
4397-53-9
Catalog Number:
AG0033WZ
Molecular Formula:
C14H12O2
Molecular Weight:
212.2439
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$19
- +
100g
98%
In Stock USA
United States
$57
- +
500g
98%
In Stock USA
United States
$225
- +
Product Description
Catalog Number:
AG0033WZ
Chemical Name:
4-Benzyloxybenzaldehyde
CAS Number:
4397-53-9
Molecular Formula:
C14H12O2
Molecular Weight:
212.2439
MDL Number:
MFCD00003387
IUPAC Name:
4-phenylmethoxybenzaldehyde
InChI:
InChI=1S/C14H12O2/c15-10-12-6-8-14(9-7-12)16-11-13-4-2-1-3-5-13/h1-10H,11H2
InChI Key:
ZVTWZSXLLMNMQC-UHFFFAOYSA-N
SMILES:
O=Cc1ccc(cc1)OCc1ccccc1
EC Number:
224-527-2
Properties
Complexity:
201  
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:
3.3  
Literature
Title Journal
Synthesis and antimicrobial evaluation of L-phenylalanine-derived C5-substituted rhodanine and chalcone derivatives containing thiobarbituric acid or 2-thioxo-4-thiazolidinone. European journal of medicinal chemistry 20121001
Novel polymer anchored Cr(III) Schiff base complexes: synthesis, characterization and antimicrobial properties. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20120901
4-[(4-Benzyl-oxybenzyl-idene)amino]-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one. Acta crystallographica. Section E, Structure reports online 20120501
(2E)-3-[3-(Benz-yloxy)phen-yl]-1-(2-hy-droxy-phen-yl)prop-2-en-1-one. Acta crystallographica. Section E, Structure reports online 20110601
(2E)-3-(3-Benzyl-oxyphen-yl)-1-(2-hydroxy-5-methyl-phen-yl)prop-2-en-1-one. Acta crystallographica. Section E, Structure reports online 20110601
Direct semi-synthesis of the anticancer lead-drug protoapigenone from apigenin, and synthesis of further new cytotoxic protoflavone derivatives. PloS one 20110101
1-Benz-yloxy-4-(2-nitro-ethen-yl)benzene. Acta crystallographica. Section E, Structure reports online 20101101
Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S beta5-subunit. The Biochemical journal 20100915
4-(Benz-yloxy)benzaldehyde. Acta crystallographica. Section E, Structure reports online 20100801
(E)-4-(Benz-yloxy)benzaldehyde thio-semicarbazone. Acta crystallographica. Section E, Structure reports online 20080601
Synthesis and preliminary evaluation of anticonvulsant activity of some [4-(benzyloxy) benzoyl]- and [4-(benzyloxy) benzyl] aminoalkanol derivatives. Acta poloniae pharmaceutica 20070101
Synthesis and antimicrobial activity of hydroxyalkyl- and hydroxyacyl-phenols and their benzyl ethers. Archiv der Pharmazie 20020301
Benzyloxybenzaldehyde analogues as novel adenylyl cyclase activators. Bioorganic & medicinal chemistry letters 20010806
Properties