Home Aldehydes 32884-23-4
32884-23-4,MFCD02113682
Catalog No.:AA00C8EL

32884-23-4 | 2-(Benzyloxy)-4-methoxybenzenecarbaldehyde

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1g
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  • 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:
AA00C8EL
Chemical Name:
2-(Benzyloxy)-4-methoxybenzenecarbaldehyde
CAS Number:
32884-23-4
Molecular Formula:
C15H14O3
Molecular Weight:
242.2699
MDL Number:
MFCD02113682
SMILES:
COc1ccc(c(c1)OCc1ccccc1)C=O
Properties
Properties
 
BP:
412.2±30.0°C at 760 mmHg  
Form:
Solid  
MP:
69-71°  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
248  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
5  
XLogP3:
2.8  

Upstream Synthesis Route

[1]ChemischeBerichte,1925,vol.58,p.1702

[1]Patent:WO2010/111353,2010,A1,.Locationinpatent:Page/Pagecolumn55-56

[2]Patent:WO2003/99793,2003,A1,.Locationinpatent:Page163

[3]JournalofNaturalProducts,2017,vol.80,#12,p.3284-3288

[4]Patent:US2018/86772,2018,A1,.Locationinpatent:Page/Pagecolumn6

[5]BioorganicandMedicinalChemistry,1998,vol.6,#9,p.1429-1437

[6]JournalofMedicinalChemistry,2009,vol.52,#15,p.4941-4945

[7]Patent:WO2010/52253,2010,A1,.Locationinpatent:Page/Pagecolumn76

[8]TetrahedronLetters,1991,vol.32,#18,p.2035-2038

[9]JournaloftheAmericanChemicalSociety,1992,vol.114,#6,p.2175-2180

[10]Chemistry-AEuropeanJournal,2011,vol.17,#9,p.2698-2703

[11]BioorganicandMedicinalChemistryLetters,2013,vol.23,#24,p.6816-6821

[12]AdvancedSynthesisandCatalysis,2013,vol.355,#14-15,p.2900-2907

[1]Patent:US6448285,2002,B1,

[1]DrugDevelopmentResearch,2016,vol.77,#1,p.37-42

[2]ChemicalandPharmaceuticalBulletin,2000,vol.48,#7,p.964-973

[3]BioorganicandMedicinalChemistry,2005,vol.13,#5,p.1537-1544

[4]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1980,p.2463-2469

[5]BulletindelaSocieteChimiquedeFrance,1960,p.1644-1646

[6]GazzettaChimicaItaliana,1989,vol.119,#2,p.87-94

[1]Patent:US2001/7873,2001,A1,

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,1980,vol.23,p.990-994

[1]JournaloftheChemicalSociety.PerkintransactionsI,1987,p.1081-1088

637-81-0    32884-23-4   
(Z)-2-Azido-3-(2-benzyloxy-4-methoxy-phenyl)-acrylicacidethylester 

[1]TetrahedronLetters,1991,vol.32,p.2035-2038

[2]JournaloftheAmericanChemicalSociety,1992,vol.114,p.2175-2180

[1]LiebigsAnnalenderChemie,1983,vol.NO.11,p.2034-2037

[1]JournaloftheChemicalSociety.PerkintransactionsI,1980,p.2463-2469

Literature

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

Journal: Bioorganic & medicinal chemistry 20050301

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Tags:32884-23-4 Molecular Formula|32884-23-4 MDL|32884-23-4 SMILES|32884-23-4 2-(Benzyloxy)-4-methoxybenzenecarbaldehyde