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3235-67-4,MFCD00461042
Catalog No.:AA003EKA

3235-67-4 | Piperidin-1-yl-acetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$19.00   $14.00
- +
5g
98%
in stock  
$77.00   $54.00
- +
100g
98%
in stock  
$1,358.00   $950.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA003EKA
Chemical Name:
Piperidin-1-yl-acetic acid
CAS Number:
3235-67-4
Molecular Formula:
C7H13NO2
Molecular Weight:
143.1836
MDL Number:
MFCD00461042
SMILES:
OC(=O)CN1CCCCC1
Properties
Properties
 
BP:
252.2°C at 760 mmHg  
Form:
Solid  
MP:
214-216℃(Solv: chloroform (67-66-3))  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
119  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
-2.5  

Downstream Synthesis Route

[1]Patent:WO2013/53983,2013,A1.Locationinpatent:Page/Pagecolumn41

[2]Patent:US2015/11548,2015,A1.Locationinpatent:Paragraph0164;0175

[3]LiebigsAnnalenderChemie,1983,p.950-961

[4]ChemischeBerichte,1909,vol.42,p.367

[5]RSCAdvances,2017,vol.7,p.47297-47308

[1]BioorganicandMedicinalChemistry,2005,vol.13,p.533-548

[2]PLoSONE,2020,vol.15

[3]ChemistryLetters,1997,p.1007-1008

[4]Patent:US2004/220412,2004,A1.Locationinpatent:Page24

[5]EuropeanJournalofMassSpectrometry,2020,vol.26,p.25-35

3235-67-4    3182-93-2   
(S)-3-Phenyl-2-(2-piperidin-1-yl-acetylamino)-propionicacidethylester 

[1]JournalofMedicinalChemistry,2000,vol.43,p.4822-4833

[1]Alanine,Alexander;Anselm,Lilli;Steward,Lucinda;Thomi,Stefan;Vifian,Walter;Groaning,MichaelD.[BioorganicandMedicinalChemistryLetters,2004,vol.14,#3,p.817-821]

[1]Patent:WO2004/82677,2004,A1.Locationinpatent:Page/Pagecolumn139

Literature

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

Journal: Bioorganic & medicinal chemistry letters 20101101

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SDS
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