Home Aldehydes 3,5-Dimethoxybenzaldehyde

3,5-Dimethoxybenzaldehyde

CAS No.:
7311-34-4
Catalog Number:
AG003INS
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%(GC)
In Stock USA
United States
$41
- +
25g
97%
In Stock USA
United States
$50
- +
100g
97%
In Stock USA
United States
$175
- +
500g
97%
In Stock USA
United States
$800
- +
Product Description
Catalog Number:
AG003INS
Chemical Name:
3,5-Dimethoxybenzaldehyde
CAS Number:
7311-34-4
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
MDL Number:
MFCD00003366
IUPAC Name:
3,5-dimethoxybenzaldehyde
InChI:
InChI=1S/C9H10O3/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-6H,1-2H3
InChI Key:
VFZRZRDOXPRTSC-UHFFFAOYSA-N
SMILES:
COc1cc(OC)cc(c1)C=O
EC Number:
230-772-6
UNII:
P82W3UJ5DT
NSC Number:
62667
Properties
Complexity:
135  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
166.063g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
166.176g/mol
Monoisotopic Mass:
166.063g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
35.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.3  
Literature
Title Journal
1-(3,5-Dimeth-oxy-benz-yl)-1H-pyrrole. Acta crystallographica. Section E, Structure reports online 20120501
trans-3,3',4,5'-Tetra-meth-oxy-stilbene. Acta crystallographica. Section E, Structure reports online 20110801
Regioselective reactions for programmable resveratrol oligomer synthesis. Nature 20110623
Antifungal activity of redox-active benzaldehydes that target cellular antioxidation. Annals of clinical microbiology and antimicrobials 20110101
Antifungal activity of resveratrol against Botrytis cinerea is improved using 2-furyl derivatives. PloS one 20110101
(E)-3,5-Dimeth-oxy-benzaldehyde oxime. Acta crystallographica. Section E, Structure reports online 20101101
Parameters of Reserpine Analogs That Induce MSH2/MSH6-Dependent Cytotoxic Response. Journal of nucleic acids 20100101
An expedient synthesis of 5-n-alkylresorcinols and novel 5-n-alkylresorcinol haptens. Beilstein journal of organic chemistry 20090101
Mechanistic kinetic model for symmetric carboligations using benzaldehyde lyase. Biotechnology and bioengineering 20080901
5,5',7,7'-Tetra-meth-oxy-2,2'-ethano-1,1'-spiro-biindane. Acta crystallographica. Section E, Structure reports online 20080201
Synthesis of the anti-Helicobacter pylori agent (+)-spirolaxine methyl ether and the unnatural (2'S)-diastereomer. Organic & biomolecular chemistry 20070821
Rational design of inhibitors of VirA-VirG two-component signal transduction. Bioorganic & medicinal chemistry letters 20070615
A methoxy derivative of resveratrol analogue selectively induced activation of the mitochondrial apoptotic pathway in transformed fibroblasts. British journal of cancer 20050214
Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents. Journal of medicinal chemistry 20040812
Cleavage of nonphenolic beta-1 diarylpropane lignin model dimers by manganese peroxidase from Phanerochaete chrysosporium. European journal of biochemistry 20030101
Properties