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67354-34-1,MFCD19388798
Catalog No.:AA00629P

67354-34-1 | Ethyl 4-(benzyloxy)-3-oxobutanoate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$7.00   $5.00
- +
1g
95%
in stock  
$7.00   $5.00
- +
5g
95%
in stock  
$17.00   $12.00
- +
10g
95%
in stock  
$32.00   $22.00
- +
25g
95%
in stock  
$73.00   $51.00
- +
100g
95%
in stock  
$278.00   $195.00
- +
  • 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:
AA00629P
Chemical Name:
Ethyl 4-(benzyloxy)-3-oxobutanoate
CAS Number:
67354-34-1
Molecular Formula:
C13H16O4
Molecular Weight:
236.2637
MDL Number:
MFCD19388798
SMILES:
CCOC(=O)CC(=O)COCc1ccccc1
Properties
Properties
 
Form:
Liquid  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
244  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
4  
Rotatable Bond Count:
8  
XLogP3:
1.7  

Upstream Synthesis Route

[1]Patent:US2003/45727,2003,A1,

[1]Patent:US2015/72982,2015,A1,.Locationinpatent:Paragraph0148;0149

[2]Patent:WO2015/38660,2015,A1,.Locationinpatent:Paragraph0187

[3]Patent:WO2016/145103,2016,A1,.Locationinpatent:Paragraph0155

[4]Patent:US2017/260189,2017,A1,.Locationinpatent:Paragraph0046;0047

[5]Tetrahedron,1978,vol.34,#2,p.223-231

[6]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1979,p.529-532

[1]JournalofMedicinalChemistry,2016,vol.59,#10,p.5051-5062

[2]JournalofOrganicChemistry,2011,vol.76,#22,p.9444-9451

[3]AngewandteChemie-InternationalEdition,2006,vol.45,#38,p.6376-6380

[4]Patent:US2012/22251,2012,A1,.Locationinpatent:Page/Pagecolumn25

[5]Patent:EP2602260,2013,A1,.Locationinpatent:Paragraph0127

[6]Patent:WO2017/12576,2017,A1,.Locationinpatent:Page/Pagecolumn120

[7]Synlett,2000,#6,p.844-846

[8]OrganicandBiomolecularChemistry,2009,vol.7,#5,p.962-975

[9]Patent:WO2015/110897,2015,A2,.Locationinpatent:Paragraph00138-00140

[10]Patent:WO2015/110897,2015,A3,.Locationinpatent:Paragraph00138-00140

[11]Patent:US2008/312255,2008,A1,.Locationinpatent:Page/Pagecolumn91

[12]NewJournalofChemistry,2016,vol.40,#10,p.8786-8808

[13]TetrahedronAsymmetry,2001,vol.12,#12,p.1713-1718

[14]EuropeanJournalofMedicinalChemistry,2015,vol.97,p.42-54

[15]Patent:US2004/19190,2004,A1,.Locationinpatent:Page38

[16]MonatsheftefuerChemie,1989,vol.120,p.891-898

[17]Synthesis,1995,#8,p.1014-1018

[18]OrganicLetters,2010,vol.12,#3,p.416-419

[19]Patent:WO2011/76878,2011,A1,.Locationinpatent:Page/Pagecolumn52-53

[20]Patent:WO2015/164308,2015,A1,.Locationinpatent:Page/Pagecolumn90

[21]ChemMedChem,2018,vol.13,#16,p.1658-1663

[1]OrganicLetters,2004,vol.6,#10,p.1657-1660

[2]JournalofOrganicChemistry,2010,vol.75,#24,p.8674-8676

[1]Patent:US2004/147561,2004,A1,.Locationinpatent:Page41

Downstream Synthesis Route

[1]Patent:US2015/72982,2015,A1.Locationinpatent:Paragraph0148;0149

[2]Patent:WO2015/38660,2015,A1.Locationinpatent:Paragraph0187

[3]Patent:WO2016/145103,2016,A1.Locationinpatent:Paragraph0155

[4]Patent:US2017/260189,2017,A1.Locationinpatent:Paragraph0046;0047

[5]Tetrahedron,1978,vol.34,p.223-231

[6]JournaloftheChemicalSociety.PerkintransactionsI,1979,p.529-532

[1]Patent:US2003/45727,2003,A1

[1]Patent:EP2602260,2013,A1

[1]Chemistry-AEuropeanJournal,2013,vol.19,p.17989-18003

67354-34-1    97-35-8   
C24H31N3O7S 

[1]Patent:WO2015/38660,2015,A1.Locationinpatent:Paragraph0196

Literature

Title: Synthesis of (+/-)-bakkenolide-A and its C-7, C-10, and C-7,10 epimers by means of an intramolecular Diels-Alder reaction.

Journal: The Journal of organic chemistry 20010615

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SDS
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