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Home Aminos (S)-(-)-2-(N-Benzylprolyl)aminobenzophenone

(S)-(-)-2-(N-Benzylprolyl)aminobenzophenone

CAS No.:
96293-17-3
Catalog Number:
AG00IJSO
Molecular Formula:
C25H24N2O2
Molecular Weight:
384.4703
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$19
- +
5g
95%
In Stock USA
United States
$75
- +
25g
95%
In Stock USA
United States
$300
- +
Product Description
Catalog Number:
AG00IJSO
Chemical Name:
(S)-(-)-2-(N-Benzylprolyl)aminobenzophenone
CAS Number:
96293-17-3
Molecular Formula:
C25H24N2O2
Molecular Weight:
384.4703
MDL Number:
MFCD00145260
IUPAC Name:
(2S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide
InChI:
InChI=1S/C25H24N2O2/c28-24(20-12-5-2-6-13-20)21-14-7-8-15-22(21)26-25(29)23-16-9-17-27(23)18-19-10-3-1-4-11-19/h1-8,10-15,23H,9,16-18H2,(H,26,29)/t23-/m0/s1
InChI Key:
IPSABLMEYFYEHS-QHCPKHFHSA-N
SMILES:
O=C([C@@H]1CCCN1Cc1ccccc1)Nc1ccccc1C(=O)c1ccccc1
Properties
Complexity:
551  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
384.184g/mol
Formal Charge:
0
Heavy Atom Count:
29  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
384.479g/mol
Monoisotopic Mass:
384.184g/mol
Rotatable Bond Count:
6  
Topological Polar Surface Area:
49.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
5.1  
Literature
Title Journal
(SP-4-4)-[Hydrogen N-({2-[(2S)-1-benzyl-pyrrolidine-2-carboxamido]phen-yl}(phen-yl)methyl-ene)-l-glutamato(2-)]nickel(II). Acta crystallographica. Section E, Structure reports online 20090401
Characterization of Ni(II) complexes of Schiff bases of amino acids and (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide using ion trap and QqTOF electrospray ionization tandem mass spectrometry. Journal of mass spectrometry : JMS 20080901
No carrier added synthesis of O-(2'-[18F]fluoroethyl)-L-tyrosine via a novel type of chiral enantiomerically pure precursor, NiII complex of a (S)-tyrosine Schiff base. Bioorganic & medicinal chemistry 20080501
Off-line combination of reversed-phase liquid chromatography and laser desorption/ionization time-of-flight mass spectrometry with seamless post-source decay fragment ion analysis for characterization of square-planar nickel(II) complexes. Journal of mass spectrometry : JMS 20060401
Enantioselectivity in Ni(II) Schiff-base complexes derived from amino-acids and (S)-o-N-(N-benzylprolyl)aminobenzophenone: molecular structure of several chiral Ni(II) Schiff-base complexes, circular dichroism and molecular mechanics studies. Dalton transactions (Cambridge, England : 2003) 20050707
Improved synthesis of proline-derived Ni(II) complexes of glycine: versatile chiral equivalents of nucleophilic glycine for general asymmetric synthesis of alpha-amino acids. The Journal of organic chemistry 20030905
Properties