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Home Other Building Blocks 5661-55-2
5661-55-2,MFCD02179052
Catalog No.:AA00EE09

5661-55-2 | 4-Phenylazetidin-2-one

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
98%
in stock  
$47.00   $33.00
- +
250mg
98%
in stock  
$77.00   $54.00
- +
1g
95%
in stock  
$172.00   $120.00
- +
5g
95%
in stock  
$710.00   $497.00
- +
10g
95%
in stock  
$1,333.00   $933.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00EE09
Chemical Name:
4-Phenylazetidin-2-one
CAS Number:
5661-55-2
Molecular Formula:
C9H9NO
Molecular Weight:
147.1739
MDL Number:
MFCD02179052
SMILES:
O=C1CC(N1)c1ccccc1
Properties
Computed Properties
 
Complexity:
161  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
Undefined Atom Stereocenter Count:
1  
XLogP3:
0.8  

Downstream Synthesis Route

[1]ChemicalCommunications,2014,vol.50,p.1698-1700

[2]Chemistry-AEuropeanJournal,2014,vol.20,p.12190-12200

[3]ChemicalCommunications,2015,vol.51,p.15588-15591

[4]ChemistryofHeterocyclicCompounds,2017,vol.53,p.329-334    Khim.Geterotsikl.Soedin.,2017,vol.53,p.329-334,6

[5]TetrahedronAsymmetry,2001,vol.12,p.2351-2358

[6]OrganicLetters,2012,vol.14,p.126-129

[7]Tetrahedron,2013,vol.69,p.1279-1284

[8]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.1500-1506

[9]EuropeanJournalofOrganicChemistry,2014,vol.2014,p.6753-6760

[10]TetrahedronLetters,1986,vol.27,p.5147-5150

[1]JournaloftheChemicalSociety.Chemicalcommunications,1983,p.959-960

[2]JournaloftheChemicalSociety.PerkintransactionsI,1993,p.2027-2046

[1]JournaloftheChemicalSociety.PerkintransactionsI,1993,p.2027-2046

[2]JournaloftheChemicalSociety.Chemicalcommunications,1983,p.959-960

[1]Begley,MichaelJ.;Crombie,Leslie;Haigh,David;Jones,RaymondC.F.;Osborne,Steven;Webster,RichardA.B.[JournaloftheChemicalSociety.PerkintransactionsI,1993,#17,p.2027-2046]

[1]TetrahedronLetters,1986,vol.27,p.5151-5154

[2]JournaloftheChemicalSociety.PerkintransactionsI,1993,p.2027-2046

Literature

Title: Monocyclic β-lactams are selective, mechanism-based inhibitors of rhomboid intramembrane proteases.

Journal: ACS chemical biology 20110415

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SDS
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