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(S)-Piperazine-2-carboxylic acid

CAS No.:
147650-70-2
Catalog Number:
AG007K3C
Molecular Formula:
C5H10N2O2
Molecular Weight:
130.1451
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
95+%
1 week
United States
$59
- +
Product Description
Catalog Number:
AG007K3C
Chemical Name:
(S)-Piperazine-2-carboxylic acid
CAS Number:
147650-70-2
Molecular Formula:
C5H10N2O2
Molecular Weight:
130.1451
MDL Number:
MFCD01318684
IUPAC Name:
(2S)-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)/t4-/m0/s1
InChI Key:
JSSXHAMIXJGYCS-BYPYZUCNSA-N
SMILES:
OC(=O)[C@@H]1CNCCN1
Properties
Complexity:
116  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
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:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-3.5  
Literature
Title Journal
A practical synthesis of differentially protected 2-(hydroxymethyl)piperazines. The Journal of organic chemistry 20071026
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
Chiral synthesis and enzymatic resolution of (S)-(-)piperazine-2-carboxylic acid using enzyme alcalase. Enantiomer 20010101
Properties