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3105-95-1,MFCD00005981
Catalog No.:AA0031Y3

3105-95-1 | L-Pipecolic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$6.00   $4.00
- +
5g
97%
in stock  
$7.00   $5.00
- +
10g
97%
in stock  
$12.00   $8.00
- +
25g
97%
in stock  
$26.00   $18.00
- +
100g
97%
in stock  
$90.00   $63.00
- +
  • 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:
AA0031Y3
Chemical Name:
L-Pipecolic acid
CAS Number:
3105-95-1
Molecular Formula:
C6H11NO2
Molecular Weight:
129.1570
MDL Number:
MFCD00005981
SMILES:
OC(=O)[C@@H]1CCCCN1
Properties
Properties
 
BP:
265.8°C at 760 mmHg  
Form:
Solid  
MP:
272 °C(lit.)  
Refractive Index:
-27 ° (C=4, H2O)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
114  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
-2.3  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,2005,vol.48,#23,p.7333-7342

[2]Chemistry-AEuropeanJournal,2010,vol.16,#25,p.7547-7553

[3]Patent:WO2015/28850,2015,A1,.Locationinpatent:Page/Pagecolumn88

[4]TetrahedronLetters,1991,vol.32,#49,p.7183-7186

[5]Patent:WO2014/19344,2014,A1,.Locationinpatent:Paragraph00601

[6]Patent:WO2014/82379,2014,A1,.Locationinpatent:Page/Pagecolumn170;171

[7]TetrahedronLetters,1990,vol.31,#16,p.2341-2344

[8]Patent:US2015/79028,2015,A1,.Locationinpatent:Paragraph1638;1654;1655;1656;1657

[1]Patent:US2006/276654,2006,A1,.Locationinpatent:Page/Pagecolumn3

[1]Patent:WO2013/91900,2013,A1,.Locationinpatent:Page/Pagecolumn41

[1]BioorganicandMedicinalChemistryLetters,2014,vol.24,#4,p.1111-1115

[2]JournaloftheAmericanChemicalSociety,2006,vol.128,#11,p.3838-3847

[3]Patent:WO2013/148478,2013,A1,.Locationinpatent:Page/Pagecolumn23

[1]BioorganicandMedicinalChemistry,2000,vol.8,#5,p.1059-1063

[2]JournalofMedicinalChemistry,2012,vol.55,#9,p.4114-4122

Downstream Synthesis Route

[1]Bioscience,BiotechnologyandBiochemistry,2006,vol.70,p.2296-2298

[2]JournalofOrganicChemistry,1990,vol.55,p.5551-5553

[3]Bioscience,BiotechnologyandBiochemistry,2002,vol.66,p.622-627

[4]TetrahedronAsymmetry,2006,vol.17,p.1775-1779

[5]JournaloftheAmericanChemicalSociety,2006,vol.128,p.3838-3847

[6]JournalofBiologicalChemistry,2010,vol.285,p.32710-32719

[7]ChemistryLetters,2012,vol.41,p.677-679

[1]JournalofOrganicChemistry,1990,vol.55,p.5551-5553

[1]JournalofOrganicChemistry,1990,vol.55,p.5551-5553

[1]JournalofOrganicChemistry,1990,vol.55,p.5551-5553

[1]JournaloftheAmericanChemicalSociety,1987,vol.109,p.5031-5033

Literature

Title: Mihalik SJ, et al. Peroxisomal L-pipecolic acid oxidation is deficient in liver from Zellweger syndrome patients. Pediatr Res. 1989 May;25(5):548-52.

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SDS
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