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Home Other Building Blocks 34371-14-7
34371-14-7,MFCD15144952
Catalog No.:AA00C0NB

34371-14-7 | 2-Deoxy-d-ribonic acid-1,4-lactone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
96%
in stock  
$48.00   $34.00
- +
1g
95%
in stock  
$98.00   $69.00
- +
5g
95%
in stock  
$296.00   $207.00
- +
10g
95%
in stock  
$461.00   $323.00
- +
25g
95%
in stock  
$909.00   $637.00
- +
100g
95%
in stock  
$2,439.00   $1,707.00
- +
  • 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:
AA00C0NB
Chemical Name:
2-Deoxy-d-ribonic acid-1,4-lactone
CAS Number:
34371-14-7
Molecular Formula:
C5H8O4
Molecular Weight:
132.1146
MDL Number:
MFCD15144952
SMILES:
OC[C@H]1OC(=O)C[C@@H]1O
Properties
Properties
 
BP:
395.3°C at 760 mmHg  
Form:
Liquid  
Storage:
Keep in dry area;-20 ℃;  

Computed Properties
 
Complexity:
122  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
-0.9  

Upstream Synthesis Route

[1]EuropeanJournalofOrganicChemistry,2013,#7,p.1306-1317

[2]Patent:US2017/57981,2017,A1,.Locationinpatent:Paragraph0268;0269;0320;0321

[3]RSCAdvances,2014,vol.4,#22,p.11023-11028

[4]Patent:WO2011/3018,2011,A2,.Locationinpatent:Page/Pagecolumn40-41

[5]Patent:WO2015/81297,2015,A1,.Locationinpatent:Paragraph00291

[1]BioorganicandMedicinalChemistryLetters,2017,vol.27,#8,p.1681-1685

[2]Tetrahedron,1993,vol.49,#2,p.349-362

[3]Patent:WO2015/164812,2015,A1,.Locationinpatent:Page/Pagecolumn64

[4]Chemistry-AEuropeanJournal,2018,vol.24,#14,p.3425-3428

[5]JournalofOrganicChemistry,2013,vol.78,#13,p.6609-6621

[6]JournalofOrganicChemistry,2007,vol.72,#10,p.3945-3948

[7]BioorganicandMedicinalChemistryLetters,1998,vol.8,#24,p.3465-3468

[8]JournaloftheAmericanChemicalSociety,1995,vol.117,#5,p.1463-1471

[9]TetrahedronAsymmetry,2001,vol.12,#3,p.387-391

[10]CanadianJournalofChemistry,2000,vol.78,#8,p.1081-1088

[11]Nucleosides,NucleotidesandNucleicAcids,2003,vol.22,#5-8,p.1183-1185

[12]OrganicLetters,2004,vol.6,#22,p.3949-3952

[13]JournalofOrganicChemistry,2006,vol.71,#19,p.7322-7328

[14]BioorganicandMedicinalChemistry,2006,vol.14,#18,p.6174-6188

[15]OrganicLetters,1999,vol.1,#8,p.1173-1175

[16]JournalofOrganicChemistry,2009,vol.74,#16,p.5779-5789

[17]JournaloftheAmericanChemicalSociety,2012,vol.134,#19,p.8090-8093

[18]OrganicLetters,2015,vol.17,#24,p.6246-6249

[19]Patent:WO2016/41877,2016,A1,.Locationinpatent:Page/Pagecolumn90

[20]JournalofMedicinalChemistry,2017,vol.60,#13,p.5424-5437

[21]Patent:CN107405356,2017,A,.Locationinpatent:Paragraph0168;0169;0170;0171;0172

[1]JournalofMedicinalChemistry,2004,vol.47,#2,p.292-295

[1]JournalofOrganicChemistry,1984,vol.49,#15,p.2762-2772

[2]Tetrahedron,1990,vol.46,#20,p.7165-7174

[3]JournaloftheAmericanChemicalSociety,1982,vol.104,#21,p.5788-5789

[4]AgriculturalandBiologicalChemistry,1985,vol.49,#5,p.1435-1440

[5]JournalofOrganicChemistry,2011,vol.76,#2,p.460-470

[1]SyntheticCommunications,1999,vol.29,#12,p.2187-2199

[2]JournaloftheChemicalSociety,ChemicalCommunications,1985,#24,p.1826-1827

Downstream Synthesis Route
2280-44-6    657-27-2    88-14-2    6338-41-6   
5-(3,4,5,6-tetrahydropyrid-3-ylidenemethyl)-2-furanmethanol 
 
1-deoxy-1-(N6-lysino)-D-fructose 
 
(+/-)-2-formyl-5-(hydroxymethyl)pyrrole-1-norleucine 
  34371-14-7 

[1]ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1984,vol.38,p.689-694

[1]BioorganicandMedicinalChemistryLetters,2017,vol.27,p.1681-1685

[2]Tetrahedron,1993,vol.49,p.349-362

[3]Patent:WO2015/164812,2015,A1.Locationinpatent:Page/Pagecolumn64

[4]Chemistry-AEuropeanJournal,2018,vol.24,p.3425-3428

[5]JournalofOrganicChemistry,2013,vol.78,p.6609-6621

[6]JournalofOrganicChemistry,2007,vol.72,p.3945-3948

[7]BioorganicandMedicinalChemistryLetters,1998,vol.8,p.3465-3468

[8]JournaloftheAmericanChemicalSociety,1995,vol.117,p.1463-1471

[9]TetrahedronAsymmetry,2001,vol.12,p.387-391

[10]CanadianJournalofChemistry,2000,vol.78,p.1081-1088

[11]Nucleosides,nucleotidesandnucleicacids,2003,vol.22,p.1183-1185

[12]OrganicLetters,2004,vol.6,p.3949-3952

[13]BioorganicandMedicinalChemistry,2006,vol.14,p.6174-6188

[14]OrganicLetters,1999,vol.1,p.1173-1175

[15]JournalofOrganicChemistry,2009,vol.74,p.5779-5789

[16]JournaloftheAmericanChemicalSociety,2012,vol.134,p.8090-8093

[17]OrganicLetters,2015,vol.17,p.6246-6249

[18]Patent:WO2016/41877,2016,A1.Locationinpatent:Page/Pagecolumn90

[19]JournalofMedicinalChemistry,2017,vol.60,p.5424-5437

[20]Patent:CN107405356,2017,A.Locationinpatent:Paragraph0168;0169;0170;0171;0172

[21]Patent:WO2020/121123,2020,A2.Locationinpatent:Paragraph0300

[1]TetrahedronLetters,1985,vol.26,p.5777-5780

[1]SyntheticCommunications,1999,vol.29,p.2187-2199

[2]JournaloftheChemicalSociety.Chemicalcommunications,1985,p.1826-1827

[1]JournalofOrganicChemistry,1984,vol.49,p.2762-2772

[2]Tetrahedron,1990,vol.46,p.7165-7174

[3]JournaloftheAmericanChemicalSociety,1982,vol.104,p.5788-5789

[4]AgriculturalandBiologicalChemistry,1985,vol.49,p.1435-1440

[5]JournalofOrganicChemistry,2011,vol.76,p.460-470

Literature
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SDS
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Tags:34371-14-7 Molecular Formula|34371-14-7 MDL|34371-14-7 SMILES|34371-14-7 2-Deoxy-d-ribonic acid-1,4-lactone