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6859-99-0,MFCD00014591
Catalog No.:AA0033NG

6859-99-0 | Piperidin-3-ol

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5g
98%
in stock  
$6.00   $4.00
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10g
98%
in stock  
$11.00   $8.00
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25g
98%
in stock  
$24.00   $17.00
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500g
98%
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$311.00   $218.00
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  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA0033NG
Chemical Name:
Piperidin-3-ol
CAS Number:
6859-99-0
Molecular Formula:
C5H11NO
Molecular Weight:
101.1469
MDL Number:
MFCD00014591
SMILES:
OC1CCCNC1
NSC Number:
62082
Properties
Properties
 
BP:
191.9°C at 760 mmHg  
Form:
Solid  
MP:
56-60 °C  
Solubility:
ethanol: 0.1 g/mL, clear  
Stability:
Air Sensitive & Hygroscopic  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
56  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Undefined Atom Stereocenter Count:
1  
XLogP3:
-0.3  

Literature

Title: Clinical pharmacokinetics and pharmacodynamics of linagliptin.

Journal: Clinical pharmacokinetics 20120701

Title: Facile syntheses of enantiopure 3-hydroxypiperidine derivatives and 3-hydroxypipecolic acids.

Journal: The Journal of organic chemistry 20100305

Title: Dihydroxylation of vinyl sulfones: stereoselective synthesis of (+)- and (-)-febrifugine and halofuginone.

Journal: The Journal of organic chemistry 20100115

Title: A concise and fully selective synthesis of the ant venom alkaloid (3S,5R,8S,9S)-3-butyl-5-propyl-8-hydroxyindolizidine.

Journal: Organic & biomolecular chemistry 20091107

Title: Complementary chemoenzymatic routes to both enantiomers of febrifugine.

Journal: Organic & biomolecular chemistry 20090721

Title: Asymmetric synthesis of (+)-isofebrifugine and (-)-sedacryptine from a common chiral nonracemic building block.

Journal: Organic letters 20080904

Title: Application of the aza-Achmatowicz oxidative rearrangement for the stereoselective synthesis of the Cassia and Prosopis alkaloid family.

Journal: The Journal of organic chemistry 20061027

Title: Methods for the synthesis of polyhydroxylated piperidines by diastereoselective dihydroxylation: exploitation in the two-directional synthesis of aza-C-linked disaccharide derivatives.

Journal: Beilstein journal of organic chemistry 20050101

Title: An aza-Achmatowicz approach toward the hydroxylated piperidine alkaloids (+/-)-azimic acid and (+/-)-deoxocassine.

Journal: Organic letters 20041028

Title: Oxidation of 3-hydroxypiperidines with iodosylbenzene in water: tandem oxidative Grob fragmentation-cyclization reaction.

Journal: Chemical & pharmaceutical bulletin 20040901

Title: [Synthesis and its application to the synthesis of biologically active natural products of new and versatile chiral building blocks].

Journal: Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20010701

Title: Efficient stereoselective synthesis of alpha-hydroxy aldehydes with (R)-piperidin-3-ol as a new chiral auxiliary.

Journal: The Journal of organic chemistry 20010406

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