Home Other Building Blocks 3-Aminopiperidin-2-one

3-Aminopiperidin-2-one

CAS No.:
1892-22-4
Catalog Number:
AG002I1S
Molecular Formula:
C5H10N2O
Molecular Weight:
114.1457
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$55
- +
5g
97%
In Stock USA
United States
$164
- +
10g
97%
In Stock USA
United States
$295
- +
25g
97%
In Stock USA
United States
$600
- +
100g
97%
In Stock USA
United States
$1750
- +
Product Description
Catalog Number:
AG002I1S
Chemical Name:
3-Aminopiperidin-2-one
CAS Number:
1892-22-4
Molecular Formula:
C5H10N2O
Molecular Weight:
114.1457
MDL Number:
MFCD06809610
IUPAC Name:
3-aminopiperidin-2-one
InChI:
InChI=1S/C5H10N2O/c6-4-2-1-3-7-5(4)8/h4H,1-3,6H2,(H,7,8)
InChI Key:
YCCMTCQQDULIFE-UHFFFAOYSA-N
SMILES:
O=C1NCCCC1N
Properties
Complexity:
103  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
114.079g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
114.148g/mol
Monoisotopic Mass:
114.079g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
55.1A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.8  
Literature
Title Journal
Synthesis of 4-substituted-3-aminopiperidin-2-ones: application to the synthesis of a conformationally constrained tetrapeptide N-acetyl-Ser-Asp-Lys-Pro. The Journal of organic chemistry 20050722
Design, synthesis and biological activity of a targeted library of potential tryptase inhibitors. Organic & biomolecular chemistry 20040607
Synthesis and evaluation of anti-apoptotic activity of L-carnitine cyclic analogues and amino acid derivatives. Farmaco (Societa chimica italiana : 1989) 20040401
Selective 3-amino-2-pyridinone acetamide thrombin inhibitors incorporating weakly basic partially saturated heterobicyclic P1-arginine mimetics. Bioorganic & medicinal chemistry letters 20031006
Three-step synthesis of (R)- and (S)-thalidomides from ornithine. Enantiomer 20010101
Properties