Home Aldehydes 34595-26-1
34595-26-1,MFCD03419311
Catalog No.:AA007DZL

34595-26-1 | 2-Piperidinobenzaldehyde

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1g
97%
in stock  
$16.00   $11.00
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5g
97%
in stock  
$46.00   $32.00
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10g
97%
in stock  
$78.00   $55.00
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25g
97%
in stock  
$180.00   $126.00
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100g
98%
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$610.00   $427.00
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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:
AA007DZL
Chemical Name:
2-Piperidinobenzaldehyde
CAS Number:
34595-26-1
Molecular Formula:
C12H15NO
Molecular Weight:
189.2536
MDL Number:
MFCD03419311
SMILES:
O=Cc1ccccc1N1CCCCC1
Properties
Computed Properties
 
Complexity:
187  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Rotatable Bond Count:
2  
XLogP3:
2.4  

Upstream Synthesis Route

[1]AngewandteChemie-InternationalEdition,2012,vol.51,#8,p.1950-1953

[2]Heterocycles,2008,vol.75,#4,p.799-838

[3]Patent:WO2004/108673,2004,A2,.Locationinpatent:Page38-39

[4]Patent:US2004/192921,2004,A1,.Locationinpatent:Page4

[5]RussianChemicalBulletin,2004,vol.53,#6,p.1240-1247

[6]ChemistryofHeterocyclicCompounds,2007,vol.43,#1,p.76-81

[7]Synthesis,2010,#24,p.4287-4299

[8]JournalofOrganicChemistry,1989,vol.54,#1,p.199-209

[9]Patent:WO2004/101540,2004,A2,.Locationinpatent:Page/Pagecolumn11-13

[10]JournalofOrganicChemistry,2009,vol.74,#19,p.7464-7469

[11]JournalofOrganicChemistry,2010,vol.75,#9,p.2893-2902

[12]OrganicandBiomolecularChemistry,2010,vol.8,#18,p.4077-4079

[13]ChemicalCommunications,2010,vol.46,#35,p.6593-6595

[14]JournalofOrganicChemistry,2011,vol.76,#1,p.342-345

[15]ChineseChemicalLetters,2012,vol.23,#4,p.395-398

[16]Tetrahedron,2013,vol.69,#34,p.7019-7025

[17]DaltonTransactions,2014,vol.43,#24,p.9098-9110

[18]Chemistry-AEuropeanJournal,2015,vol.21,#4,p.1632-1636

[19]JournalofOrganicChemistry,2014,vol.79,#21,p.10434-10446

[20]OrganicLetters,2017,vol.19,#7,p.1566-1569

[21]Patent:US2018/258076,2018,A1,.Locationinpatent:Paragraph0496

[1]EuropeanJournalofOrganicChemistry,2015,vol.2015,#18,p.4018-4023

[1]JournalofMedicinalChemistry,1998,vol.41,#26,p.5219-5246

[1]Chemistry-AEuropeanJournal,2012,vol.18,#1,p.68-71

[1]JournalofMedicinalChemistry,1998,vol.41,#26,p.5219-5246

Downstream Synthesis Route

[1]AngewandteChemie-InternationalEdition,2012,vol.51,p.1950-1953

[2]Heterocycles,2008,vol.75,p.799-838

[3]Patent:WO2004/108673,2004,A2.Locationinpatent:Page38-39

[4]Patent:CN109970681,2019,A.Locationinpatent:Paragraph0043-0045

[5]Patent:US2004/192921,2004,A1.Locationinpatent:Page4

[6]RussianChemicalBulletin,2004,vol.53,p.1240-1247

[7]ChemistryofHeterocyclicCompounds,2007,vol.43,p.76-81

[8]OrganicLetters,2019,vol.21,p.8290-8294

[9]Synthesis,2010,p.4287-4299

[10]JournalofOrganicChemistry,2019,vol.84,p.9671-9683

[11]JournalofOrganicChemistry,1989,vol.54,p.199-209

[12]Patent:WO2004/101540,2004,A2.Locationinpatent:Page/Pagecolumn11-13

[13]JournalofOrganicChemistry,2009,vol.74,p.7464-7469

[14]ChemicalCommunications,2010,vol.46,p.6593-6595

[15]JournalofOrganicChemistry,2011,vol.76,p.342-345

[16]ChineseChemicalLetters,2012,vol.23,p.395-398

[17]Tetrahedron,2013,vol.69,p.7019-7025

[18]DaltonTransactions,2014,vol.43,p.9098-9110

[19]Chemistry-AEuropeanJournal,2015,vol.21,p.1632-1636

[20]JournalofOrganicChemistry,2014,vol.79,p.10434-10446

[21]OrganicLetters,2017,vol.19,p.1566-1569

[22]Patent:US2018/258076,2018,A1.Locationinpatent:Paragraph0496

[23]Patent:JP2018/199673,2018,A.Locationinpatent:Paragraph0170

[24]OrganicLetters,2019,vol.21,p.3990-3993

[25]Tetrahedron,2019,vol.75

[1]Synthesis,1982,p.662-665

ethyltriphenylphosphoniumbromide 
  34595-26-1    83716-71-6 

[1]Synthesis,1982,p.662-665

[1]Synthesis,1982,p.662-665

34595-26-1   
C22H24BrP 
  83716-73-8 

[1]Synthesis,1982,p.662-665

Literature
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