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3057-74-7,MFCD06809742
Catalog No.:AA0037MB

3057-74-7 | L-Aspartic acid 4-tert-butyl ester

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1g
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$6.00   $4.00
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5g
98%
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$13.00   $9.00
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25g
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$40.00   $28.00
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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:
AA0037MB
Chemical Name:
L-Aspartic acid 4-tert-butyl ester
CAS Number:
3057-74-7
Molecular Formula:
C8H15NO4
Molecular Weight:
189.2090
MDL Number:
MFCD06809742
SMILES:
N[C@H](C(=O)O)CC(=O)OC(C)(C)C
Properties
Properties
 
BP:
318.7°C at 760 mmHg  
Form:
Solid  
MP:
220 °C (dec.)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
207  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
5  
XLogP3:
-1.4  

Upstream Synthesis Route

[1]Patent:US2010/16631,2010,A1,.Locationinpatent:Page/Pagecolumn5-6

[2]BioorganicandMedicinalChemistryLetters,2012,vol.22,#15,p.4975-4978

[3]Patent:WO2017/24009,2017,A1,.Locationinpatent:Paragraph0652

[4]RussianJournalofBioorganicChemistry,1999,vol.25,#5,p.283-287

[5]BioorganicheskayaKhimiya,1999,vol.25,#5,p.323-328

[1]JournaloftheChemicalSociety[Section]C:Organic,1967,p.2632-2636

[1]HelveticaChimicaActa,1963,vol.46,p.1975-1996

[2]ChemischeBerichte,1972,vol.105,#11,p.3650-3657

[3]Tetrahedron,1972,vol.28,p.2649-2654

[1]JournalofOrganicChemistry,1963,vol.28,p.1251-1253

[1]SyntheticCommunications,2009,vol.39,#11,p.2022-2031

[2]ChemicalandPharmaceuticalBulletin,1996,vol.44,#11,p.2189-2191

Downstream Synthesis Route

[1]HelveticaChimicaActa,1963,vol.46,p.1975-1996

[2]ChemischeBerichte,1972,vol.105,p.3650-3657

[1]JournaloftheChemicalSocietyC:Organic,1967,p.2632-2636

[1]Synthesis,2011,p.2893-2896

[2]Tetrahedron,1972,vol.28,p.2649-2654

[3]ChemischeBerichte,1972,vol.105,p.3650-3657

[1]Kapurniotu,Afroditi;Voelter,Wolfgang[LiebigsAnnalenderChemie,1991,#12,p.1251-1258]

[1]JournalofMedicinalChemistry,1992,vol.35,p.4914-4917

Literature

Title: Asymmetric synthesis of trans-2,3-piperidinedicarboxylic acid and trans-3,4-piperidinedicarboxylic acid derivatives.

Journal: The Journal of organic chemistry 20020208

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SDS
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