Home Other Building Blocks Piperidin-3-ol

Piperidin-3-ol

CAS No.:
6859-99-0
Catalog Number:
AG0033Q8
Molecular Formula:
C5H11NO
Molecular Weight:
101.1469
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$38
- +
100g
98%
In Stock USA
United States
$119
- +
500g
98%
In Stock USA
United States
$425
- +
Product Description
Catalog Number:
AG0033Q8
Chemical Name:
Piperidin-3-ol
CAS Number:
6859-99-0
Molecular Formula:
C5H11NO
Molecular Weight:
101.1469
MDL Number:
MFCD00014591
IUPAC Name:
piperidin-3-ol
InChI:
InChI=1S/C5H11NO/c7-5-2-1-3-6-4-5/h5-7H,1-4H2
InChI Key:
BIWOSRSKDCZIFM-UHFFFAOYSA-N
SMILES:
OC1CCCNC1
EC Number:
229-957-4
NSC Number:
62082
Properties
Complexity:
56  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
101.084g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
101.149g/mol
Monoisotopic Mass:
101.084g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
32.3A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.3  
Literature
Title Journal
Clinical pharmacokinetics and pharmacodynamics of linagliptin. Clinical pharmacokinetics 20120701
Facile syntheses of enantiopure 3-hydroxypiperidine derivatives and 3-hydroxypipecolic acids. The Journal of organic chemistry 20100305
Dihydroxylation of vinyl sulfones: stereoselective synthesis of (+)- and (-)-febrifugine and halofuginone. The Journal of organic chemistry 20100115
A concise and fully selective synthesis of the ant venom alkaloid (3S,5R,8S,9S)-3-butyl-5-propyl-8-hydroxyindolizidine. Organic & biomolecular chemistry 20091107
Complementary chemoenzymatic routes to both enantiomers of febrifugine. Organic & biomolecular chemistry 20090721
Asymmetric synthesis of (+)-isofebrifugine and (-)-sedacryptine from a common chiral nonracemic building block. Organic letters 20080904
Application of the aza-Achmatowicz oxidative rearrangement for the stereoselective synthesis of the Cassia and Prosopis alkaloid family. The Journal of organic chemistry 20061027
Methods for the synthesis of polyhydroxylated piperidines by diastereoselective dihydroxylation: exploitation in the two-directional synthesis of aza-C-linked disaccharide derivatives. Beilstein journal of organic chemistry 20050101
An aza-Achmatowicz approach toward the hydroxylated piperidine alkaloids (+/-)-azimic acid and (+/-)-deoxocassine. Organic letters 20041028
Oxidation of 3-hydroxypiperidines with iodosylbenzene in water: tandem oxidative Grob fragmentation-cyclization reaction. Chemical & pharmaceutical bulletin 20040901
[Synthesis and its application to the synthesis of biologically active natural products of new and versatile chiral building blocks]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20010701
Efficient stereoselective synthesis of alpha-hydroxy aldehydes with (R)-piperidin-3-ol as a new chiral auxiliary. The Journal of organic chemistry 20010406
Properties