Home Aldehydes 123387-72-4
123387-72-4,MFCD08064267
Catalog No.:AA000KEY

123387-72-4 | N-Boc-(methylamino)acetaldehyde

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250mg
95%
in stock  
$6.00   $4.00
- +
1g
95%
in stock  
$7.00   $5.00
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5g
95%
in stock  
$13.00   $9.00
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10g
95%
in stock  
$23.00   $16.00
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25g
95%
in stock  
$46.00   $32.00
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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:
AA000KEY
Chemical Name:
N-Boc-(methylamino)acetaldehyde
CAS Number:
123387-72-4
Molecular Formula:
C8H15NO3
Molecular Weight:
173.2096
MDL Number:
MFCD08064267
SMILES:
O=CCN(C(=O)OC(C)(C)C)C
Properties
Computed Properties
 
Complexity:
172  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
4  
XLogP3:
0.6  

Upstream Synthesis Route

[1]Patent:WO2007/120098,2007,A1,.Locationinpatent:Page/Pagecolumn88

[2]Patent:WO2013/68552,2013,A1,.Locationinpatent:Page/Pagecolumn53

[3]ChemMedChem,2015,vol.10,#3,p.470-489

[4]Patent:WO2011/133039,2011,A2,.Locationinpatent:Page/Pagecolumn202

[5]JournaloftheChemicalSociety-PerkinTransactions1,1997,#21,p.3219-3225

[6]Patent:WO2006/135316,2006,A1,.Locationinpatent:Page/Pagecolumn124-125

[7]Patent:WO2009/29439,2009,A1,.Locationinpatent:Page/Pagecolumn16

[8]JournaloftheAmericanChemicalSociety,2010,vol.132,#47,p.16962-16976

[9]Patent:EP2287173,2011,A1,.Locationinpatent:Page/Pagecolumn43

[10]Tetrahedron,2011,vol.67,#34,p.6131-6137

[11]Patent:WO2013/68554,2013,A1,.Locationinpatent:Page/Pagecolumn63

[1]EuropeanJournalofMedicinalChemistry,1991,vol.26,#9,p.921-928

[2]Tetrahedron,2002,vol.58,#9,p.1719-1737

[3]JournalofNaturalProducts,2003,vol.66,#2,p.183-199

[4]Patent:US2006/235037,2006,A1,.Locationinpatent:Page/Pagecolumn19

[1]HelveticaChimicaActa,2006,vol.89,#8,p.1559-1573

[2]JournaloftheChemicalSociety-PerkinTransactions1,1997,#21,p.3219-3225

[3]Tetrahedron,2011,vol.67,#34,p.6131-6137

[4]Patent:WO2011/133039,2011,A2,

[5]ChemMedChem,2015,vol.10,#3,p.470-489

[1]JournalofNaturalProducts,2003,vol.66,#2,p.183-199

[2]Tetrahedron,2002,vol.58,#9,p.1719-1737

[3]EuropeanJournalofMedicinalChemistry,1991,vol.26,#9,p.921-928

[1]Patent:US5888972,1999,A,

Downstream Synthesis Route

[1]Patent:WO2007/120098,2007,A1.Locationinpatent:Page/Pagecolumn88

[2]Patent:WO2013/68552,2013,A1.Locationinpatent:Page/Pagecolumn53

[3]ChemMedChem,2015,vol.10,p.470-489

[4]BioorganicandMedicinalChemistry,2020,vol.28

[5]Patent:WO2011/133039,2011,A2.Locationinpatent:Page/Pagecolumn202

[6]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.3219-3225

[7]Patent:WO2006/135316,2006,A1.Locationinpatent:Page/Pagecolumn124-125

[8]Patent:WO2009/29439,2009,A1.Locationinpatent:Page/Pagecolumn16

[9]JournaloftheAmericanChemicalSociety,2010,vol.132,p.16962-16976

[10]Patent:EP2287173,2011,A1.Locationinpatent:Page/Pagecolumn43

[11]Tetrahedron,2011,vol.67,p.6131-6137

[12]Patent:WO2013/68554,2013,A1.Locationinpatent:Page/Pagecolumn63

[13]Patent:CN109106951,2019,A.Locationinpatent:Paragraph0145;0146;0147;0148

[14]Patent:US2019/345139,2019,A1.Locationinpatent:Paragraph0596-0597

[1]HelveticaChimicaActa,2006,vol.89,p.1559-1573

[1]HelveticaChimicaActa,2006,vol.89,p.1559-1573

[1]JournalofNaturalProducts,2003,vol.66,p.183-199

[1]Patent:US2010/173889,2010,A1.Locationinpatent:Page/Pagecolumn64

Literature
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SDS
Tags:123387-72-4 Molecular Formula|123387-72-4 MDL|123387-72-4 SMILES|123387-72-4 N-Boc-(methylamino)acetaldehyde