sales@angenesci.com
Login | Register
logo
Structures Search
Home Carboxys (R)-Piperidine-2-carboxylic acid

(R)-Piperidine-2-carboxylic acid

CAS No.:
1723-00-8
Catalog Number:
AG0032E2
Molecular Formula:
C6H11NO2
Molecular Weight:
129.1570
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$15
- +
25g
98%
In Stock USA
United States
$50
- +
100g
98%
In Stock USA
United States
$150
- +
500g
98%
In Stock USA
United States
$675
- +
Product Description
Catalog Number:
AG0032E2
Chemical Name:
(R)-Piperidine-2-carboxylic acid
CAS Number:
1723-00-8
Molecular Formula:
C6H11NO2
Molecular Weight:
129.1570
MDL Number:
MFCD00064346
IUPAC Name:
(2R)-piperidine-2-carboxylic acid
InChI:
InChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m1/s1
InChI Key:
HXEACLLIILLPRG-RXMQYKEDSA-N
SMILES:
OC(=O)C1CCCCN1
EC Number:
217-024-4
UNII:
XPO6784Z20
Properties
Complexity:
114  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
129.079g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
129.159g/mol
Monoisotopic Mass:
129.079g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
49.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-2.3  
Literature
Title Journal
Enantioselective allylation of imines catalyzed by newly developed (-)-β-pinene-based π-allylpalladium catalyst: an efficient synthesis of (R)-α-propylpiperonylamine and (R)-pipecolic acid. Organic & biomolecular chemistry 20121014
An efficient synthesis of enantiomerically pure (R)-pipecolic acid, (S)-proline, and their N-alkylated derivatives. The Journal of organic chemistry 20070302
Properties