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87219-29-2,MFCD00216569
Catalog No.:AA003691

87219-29-2 | Benzyl (S)-(-)-tetrahydro-5-oxo-3-furanylcarbamate

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100mg
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$6.00   $4.00
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250mg
97%
in stock  
$7.00   $5.00
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1g
97%
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$12.00   $8.00
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5g
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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:
AA003691
Chemical Name:
Benzyl (S)-(-)-tetrahydro-5-oxo-3-furanylcarbamate
CAS Number:
87219-29-2
Molecular Formula:
C12H13NO4
Molecular Weight:
235.2359
MDL Number:
MFCD00216569
SMILES:
O=C(N[C@@H]1COC(=O)C1)OCc1ccccc1
Properties
Properties
 
BP:
466°C at 760 mmHg  
Form:
Solid  
MP:
103-105 °C(lit.);  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
286  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
1.1  

Upstream Synthesis Route

[1]TetrahedronLetters,1983,vol.24,#27,p.2733-2736

[2]JournaloftheAmericanChemicalSociety,1986,vol.108,#16,p.4943-4952

[3]JournaloftheChemicalSociety,PerkinTransactions1:OrganicandBio-OrganicChemistry(1972-1999),1990,#2,p.432-433

[4]OrganicandBiomolecularChemistry,2004,vol.2,#15,p.2181-2187

[5]ChemicalandPharmaceuticalBulletin,1986,vol.34,#7,p.3020-3024

[6]JournalofOrganicChemistry,1994,vol.59,#9,p.2349-2357

[7]Synlett,2003,#6,p.797-800

[1]Tetrahedron,2016,vol.72,#46,p.7268-7275

[2]Tetrahedron,2016,vol.72,#46,p.7268-7275

[1]OrganicandBiomolecularChemistry,2004,vol.2,#15,p.2181-2187

[2]OrganicandBiomolecularChemistry,2003,vol.1,#2,p.247-250

[3]Synlett,2003,#6,p.797-800

[4]JournalofOrganicChemistry,1994,vol.59,#9,p.2349-2357

[5]JournaloftheAmericanChemicalSociety,1986,vol.108,#16,p.4943-4952

[6]ChemicalandPharmaceuticalBulletin,1986,vol.34,#7,p.3020-3024

[7]TetrahedronLetters,1983,vol.24,#27,p.2733-2736

[1]OrganicandBiomolecularChemistry,2004,vol.2,#14,p.2003-2011

[1]JournaloftheAmericanChemicalSociety,2015,vol.137,#11,p.3767-3770

[2]JournaloftheAmericanChemicalSociety,2015,vol.137,#11,p.3767-3770

Downstream Synthesis Route

[1]Tetrahedron,1992,vol.48,p.4231-4238

[1]ChemicalandPharmaceuticalBulletin,1986,vol.34,p.3020-3024

[1]OrganicandBiomolecularChemistry,2004,vol.2,p.2181-2187

[2]OrganicandBiomolecularChemistry,2003,vol.1,p.247-250

[3]Synlett,2003,p.797-800

[4]JournalofOrganicChemistry,1994,vol.59,p.2349-2357

[5]JournaloftheAmericanChemicalSociety,1986,vol.108,p.4943-4952

[6]ChemicalandPharmaceuticalBulletin,1986,vol.34,p.3020-3024

[7]TetrahedronLetters,1983,vol.24,p.2733-2736

[1]OrganicandBiomolecularChemistry,2004,vol.2,p.2181-2187

[1]OrganicandBiomolecularChemistry,2004,vol.2,p.2181-2187

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: 3-D-QSAR of N-substituted 4-amino-3,3-dialkyl-2(3H)-furanone GABA receptor modulators using molecular field analysis and receptor surface modelling study.

Journal: Bioorganic & medicinal chemistry letters 20040105

Title: N-Substituted 4-amino-3,3-dipropyl-2(3H)-furanones: new positive allosteric modulators of the GABA(A) receptor sharing electrophysiological properties with the anticonvulsant loreclezole.

Journal: Journal of medicinal chemistry 20020620

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SDS
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