Home Aldehydes 7311-34-4
7311-34-4,MFCD00003366
Catalog No.:AA003IL0

7311-34-4 | 3,5-Dimethoxybenzaldehyde

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$6.00   $4.00
- +
5g
97%
in stock  
$7.00   $5.00
- +
10g
97%
in stock  
$13.00   $9.00
- +
25g
97%
in stock  
$19.00   $13.00
- +
500g
97%
in stock  
$360.00   $252.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003IL0
Chemical Name:
3,5-Dimethoxybenzaldehyde
CAS Number:
7311-34-4
Molecular Formula:
C9H10O3
Molecular Weight:
166.1739
MDL Number:
MFCD00003366
SMILES:
COc1cc(OC)cc(c1)C=O
NSC Number:
62667
Properties
Properties
 
BP:
151°C at 760 mmHg  
Form:
Solid  
MP:
45-48 °C(lit.)  
Refractive Index:
1.5260 (estimate)  
Stability:
Air Sensitive  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
135  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
3  
XLogP3:
1.3  

Upstream Synthesis Route

[1]Synthesis,1989,#6,p.451-452

[2]JournalofOrganicChemistry,2015,vol.80,#17,p.8657-8667

[3]JournalofHeterocyclicChemistry,2009,vol.46,#5,p.980-987

[1]JournalofMedicinalChemistry,2006,vol.49,#21,p.6197-6208

[1]Patent:CN107951870,2018,A,.Locationinpatent:Paragraph0032;0037;0038

[1]Patent:US2013/281399,2013,A1,.Locationinpatent:Paragraph0791;0797

[2]EuropeanJournalofOrganicChemistry,2018,vol.2018,#40,p.5605-5614

[3]JournalofOrganicChemistry,1985,vol.50,#13,p.2236-2240

[4]Patent:US2014/309427,2014,A1,.Locationinpatent:Paragraph0097;0098;0099;0100

[5]PLoSONE,2015,vol.10,#10,

[6]Patent:EP1386913,2004,A1,.Locationinpatent:Page65-66

[7]Patent:WO2016/14529,2016,A1,.Locationinpatent:Page/Pagecolumn25

[1]Patent:US9238640,2016,B2,.Locationinpatent:Page/Pagecolumn151;152;153

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.PerkintransactionsI,1981,p.471-479

[2]JournalfurpraktischeChemie(Leipzig1954),1925,vol.<2>110,p.127

[3]FreeRadicalBiologyandMedicine,2011,vol.50,p.1447-1457

[4]BioorganicandMedicinalChemistry,2016,vol.24,p.1495-1503

[5]JournalofEnzymeInhibitionandMedicinalChemistry,2020,vol.35,p.72-84

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1924,p.2    ChemischesZentralblatt,1925,vol.96,p.1713

[1]Tetrahedron,2007,vol.63,p.9382-9386

[2]Journalofagriculturalandfoodchemistry,2002,vol.50,p.2748-2754

[3]JournalofOrganicChemistry,1964,vol.29,p.435-439

[4]AustralianJournalofChemistry,1973,vol.26,p.2277-2290

[1]TetrahedronLetters,1980,vol.21,p.5089-5090

3222-48-8    7311-34-4    77784-14-6    77784-13-5   
2,4-bis(3',5'-dimethoxybenzoyl)-6-methylpyridine-3-carbonitrile 

[1]AustralianJournalofChemistry,1982,vol.35,p.1451-1468

Literature

Title: 1-(3,5-Dimeth-oxy-benz-yl)-1H-pyrrole.

Journal: Acta crystallographica. Section E, Structure reports online 20120501

Title: trans-3,3',4,5'-Tetra-meth-oxy-stilbene.

Journal: Acta crystallographica. Section E, Structure reports online 20110801

Title: Regioselective reactions for programmable resveratrol oligomer synthesis.

Journal: Nature 20110623

Title: Antifungal activity of redox-active benzaldehydes that target cellular antioxidation.

Journal: Annals of clinical microbiology and antimicrobials 20110101

Title: Antifungal activity of resveratrol against Botrytis cinerea is improved using 2-furyl derivatives.

Journal: PloS one 20110101

Title: (E)-3,5-Dimeth-oxy-benzaldehyde oxime.

Journal: Acta crystallographica. Section E, Structure reports online 20101101

Title: Parameters of Reserpine Analogs That Induce MSH2/MSH6-Dependent Cytotoxic Response.

Journal: Journal of nucleic acids 20100101

Title: An expedient synthesis of 5-n-alkylresorcinols and novel 5-n-alkylresorcinol haptens.

Journal: Beilstein journal of organic chemistry 20090101

Title: Mechanistic kinetic model for symmetric carboligations using benzaldehyde lyase.

Journal: Biotechnology and bioengineering 20080901

Title: 5,5',7,7'-Tetra-meth-oxy-2,2'-ethano-1,1'-spiro-biindane.

Journal: Acta crystallographica. Section E, Structure reports online 20080201

Title: Synthesis of the anti-Helicobacter pylori agent (+)-spirolaxine methyl ether and the unnatural (2'S)-diastereomer.

Journal: Organic & biomolecular chemistry 20070821

Title: Rational design of inhibitors of VirA-VirG two-component signal transduction.

Journal: Bioorganic & medicinal chemistry letters 20070615

Title: A methoxy derivative of resveratrol analogue selectively induced activation of the mitochondrial apoptotic pathway in transformed fibroblasts.

Journal: British journal of cancer 20050214

Title: Concise synthesis and structure-activity relationships of combretastatin A-4 analogues, 1-aroylindoles and 3-aroylindoles, as novel classes of potent antitubulin agents.

Journal: Journal of medicinal chemistry 20040812

Title: Cleavage of nonphenolic beta-1 diarylpropane lignin model dimers by manganese peroxidase from Phanerochaete chrysosporium.

Journal: European journal of biochemistry 20030101

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:7311-34-4 Molecular Formula|7311-34-4 MDL|7311-34-4 SMILES|7311-34-4 3,5-Dimethoxybenzaldehyde |Organic_Building_Blocks