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13500-53-3,MFCD12407103
Catalog No.:AA006ZHD

13500-53-3 | (2S,4R)-Dibenzyl 4-hydroxypyrrolidine-1,2-dicarboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$74.00   $52.00
- +
1g
95%
in stock  
$103.00   $72.00
- +
5g
95%
in stock  
$346.00   $242.00
- +
  • 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:
AA006ZHD
Chemical Name:
(2S,4R)-Dibenzyl 4-hydroxypyrrolidine-1,2-dicarboxylate
CAS Number:
13500-53-3
Molecular Formula:
C20H21NO5
Molecular Weight:
355.3844
MDL Number:
MFCD12407103
SMILES:
O[C@H]1CN([C@@H](C1)C(=O)OCc1ccccc1)C(=O)OCc1ccccc1
Properties
Computed Properties
 
Complexity:
471  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
26  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
7  
XLogP3:
2.6  

Upstream Synthesis Route

[1]AdvancedSynthesisandCatalysis,2008,vol.350,#17,p.2747-2760

[2]JournalofOrganicChemistry,2001,vol.66,#3,p.1038-1042

[3]AngewandteChemie-InternationalEdition,2007,vol.46,#47,p.9073-9077

[4]Synlett,1999,#9,p.1465-1467

[5]Tetrahedron,2008,vol.64,#10,p.2480-2488

[6]AngewandteChemie-InternationalEdition,2008,vol.47,#44,p.8429-8432

[7]AdvancedSynthesisandCatalysis,2010,vol.352,#1,p.108-112

[8]TetrahedronLetters,1994,vol.35,#3,p.451-454

[9]ChemicalandPharmaceuticalBulletin,2018,vol.66,#5,p.575-580

[10]JournalofOrganicChemistry,2017,vol.82,#23,p.12366-12376

[11]Tetrahedron,1998,vol.54,#5-6,p.981-996

[12]JournalofOrganicChemistry,2006,vol.71,#13,p.5004-5007

[13]Synlett,2010,#13,p.1943-1946

[14]JournalofMolecularCatalysisA:Chemical,2012,vol.363-364,p.404-410,7

[15]JournalofOrganicChemistry,1991,vol.56,#8,p.2787-2800

[16]CarbohydrateResearch,1996,vol.286,p.123-138

[17]BioorganicandMedicinalChemistryLetters,2008,vol.18,#3,p.1096-1101

[18]Synlett,2011,#4,p.503-507

[19]Macromolecules,2010,vol.43,#15,p.6374-6380

[20]Patent:US2013/65935,2013,A1,.Locationinpatent:Paragraph0097;0098

[21]Patent:WO2018/20358,2018,A1,.Locationinpatent:Page/Pagecolumn85

[1]JournalofOrganicChemistry,2004,vol.69,#23,p.8077-8085

[1]AdvancedSynthesisandCatalysis,2005,vol.347,#10,p.1395-1403

[1]JournalofOrganicChemistry,2007,vol.72,#24,p.9353-9356

[1]JournalofOrganicChemistry,2006,vol.71,#13,p.5004-5007

[2]TetrahedronLetters,1994,vol.35,#3,p.451-454

[3]JournalofOrganicChemistry,1991,vol.56,#8,p.2787-2800

[4]CanadianJournalofBiochemistryandPhysiology,1959,vol.37,p.583,584

[5]Synlett,2011,#4,p.503-507

[6]Macromolecules,2010,vol.43,#15,p.6374-6380

[7]JournalofMolecularCatalysisA:Chemical,2012,vol.363-364,p.404-410,7

[8]JournalofOrganicChemistry,2017,vol.82,#23,p.12366-12376

[9]Patent:WO2018/20358,2018,A1,

[10]ChemicalandPharmaceuticalBulletin,2018,vol.66,#5,p.575-580

[11]Patent:US2013/65935,2013,A1,

Downstream Synthesis Route
1‑(1‑carboxymethyl)‑3‑methylimidazoliumtetrafluoroborate 
  13500-53-3   
C26H28N3O6(1+)*BF4(1-) 

[1]AdvancedSynthesisandCatalysis,2006,vol.348,p.1711-1718

n-octyl(diisopropyl)chlorosilane 
  13500-53-3   
N-benzyloxycarbonyl-4(S)-diisopropyloctylsilyloxy-L-proline 

[1]ChemicalCommunications,2006,p.4291-4293

[1]AngewandteChemie-InternationalEdition,2006,vol.45,p.958-961

[1]JournalofOrganicChemistry,2007,vol.72,p.9353-9356

24801-88-5    13500-53-3   
(2S,4R)-1,2-dibenzyloxycarbonyl-4-(3-triethoxysilylpropylaminocarbonyloxy)pyrrolidine 

[1]JournalofOrganicChemistry,2007,vol.72,p.9353-9356

[2]JournalofMolecularCatalysisA:Chemical,2012,vol.363-364,p.404-410,7

[3]RSCAdvances,2014,vol.4,p.9292-9299

Literature
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SDS
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Tags:13500-53-3 Molecular Formula|13500-53-3 MDL|13500-53-3 SMILES|13500-53-3 (2S,4R)-Dibenzyl 4-hydroxypyrrolidine-1,2-dicarboxylate