Home Carboxys Piperazine-2-carboxylic acid

Piperazine-2-carboxylic acid

CAS No.:
2762-32-5
Catalog Number:
AG002U9G
Molecular Formula:
C5H10N2O2
Molecular Weight:
130.1451
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$32
- +
100g
98%
In Stock USA
United States
$107
- +
500g
98%
In Stock USA
United States
$407
- +
Product Description
Catalog Number:
AG002U9G
Chemical Name:
Piperazine-2-carboxylic acid
CAS Number:
2762-32-5
Molecular Formula:
C5H10N2O2
Molecular Weight:
130.1451
MDL Number:
MFCD00132878
IUPAC Name:
piperazine-2-carboxylic acid
InChI:
InChI=1S/C5H10N2O2/c8-5(9)4-3-6-1-2-7-4/h4,6-7H,1-3H2,(H,8,9)
InChI Key:
JSSXHAMIXJGYCS-UHFFFAOYSA-N
SMILES:
OC(=O)C1CNCCN1
Properties
Complexity:
116  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
130.074g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
130.147g/mol
Monoisotopic Mass:
130.074g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
61.4A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-3.5  
Literature
Title Journal
High-performance liquid chromatographic enantioseparation of unusual secondary amino acids on a D-penicillamine-based chiral ligand exchange column. Chirality 20060801
S-stereoselective piperazine-2-tert-butylcarboxamide hydrolase from Pseudomonas azotoformans IAM 1603 is a novel L-amino acid amidase. European journal of biochemistry 20040401
A novel R-stereoselective amidase from Pseudomonas sp. MCI3434 acting on piperazine-2-tert-butylcarboxamide. European journal of biochemistry 20040401
Application of a new chiral derivatizing agent to the enantioseparation of secondary amino acids. Journal of chromatography. A 20020301
Chiral synthesis and enzymatic resolution of (S)-(-)piperazine-2-carboxylic acid using enzyme alcalase. Enantiomer 20010101
Properties