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Home > Nitro Compounds > 7495-01-4
7495-01-4 | N-3-5-DINITROBENZOYL-L-LEUCINE
CAS No: 7495-01-4 Catalog No: AG00GFKZ MDL No:
Product Description
Catalog Number:
AG00GFKZ
Chemical Name:
N-3-5-DINITROBENZOYL-L-LEUCINE
CAS Number:
7495-01-4
IUPAC Name:
(2S)-2-[(3,5-dinitrobenzoyl)amino]-4-methylpentanoic acid
InChI:
InChI=1S/C13H15N3O7/c1-7(2)3-11(13(18)19)14-12(17)8-4-9(15(20)21)6-10(5-8)16(22)23/h4-7,11H,3H2,1-2H3,(H,14,17)(H,18,19)/t11-/m0/s1
InChI Key:
DIOBIOPCRMWGAT-NSHDSACASA-N
Properties
Complexity:
461
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Exact Mass:
325.091g/mol
Formal Charge:
0
Heavy Atom Count:
23
Hydrogen Bond Acceptor Count:
7
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
325.277g/mol
Monoisotopic Mass:
325.091g/mol
Rotatable Bond Count:
5
Topological Polar Surface Area:
158A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.2
Literature
| Title | Journal |
|---|---|
| Retention of fluorinated chiral selectors in biphasic fluorinated solvent systems and its application to the separation of enantiomers by countercurrent chromatography. | Journal of chromatography. A 20100212 |
| Multiple dual-mode countercurrent chromatography applied to chiral separations using a (S)-naproxen derivative as chiral selector. | Journal of chromatography. A 20091127 |
| Solvation of phenylglycine- and leucine-derived chiral stationary phases: molecular dynamics simulation study. | The journal of physical chemistry. B 20081016 |
| Surface plasmon resonance spectroscopic chiral discrimination using self-assembled leucine derivative monolayer. | Talanta 20080630 |
| Preparation and evaluation of a new synthetic polymeric chiral stationary phase for HPLC based on the trans-9,10-dihydro-9,10-ethanoanthracene-(11S,12S)-11,12-dicarboxylic acid bis-4-vinylphenylamide monomer. | Analytical and bioanalytical chemistry 20070401 |
| Extended application of a chiral stationary phase based on (+)-(1 8-crown-6)-2,3,11,12-tetracarboxylic acid to the resolution of N-(substituted benzoyl)-alpha-amino acid amides. | Journal of separation science 20060701 |
| Application of cellulose and amylose arylcarbamates as chiral selectors in counter-current chromatography. | Journal of chromatography. A 20060224 |
| Deuterium isotope effects observed during competitive binding chiral recognition electrospray ionization--mass spectrometry of cinchona alkaloid-based systems. | Journal of mass spectrometry : JMS 20060201 |
| Tertiary amine appended derivatives of N-(3,5-dinitrobenzoyl)leucine as chiral selectors for enantiomer assays by electrospray ionization mass spectrometry. | Analytical chemistry 20050801 |
| Study of the racemization observed in the amide bond forming reaction on silica gel. | Journal of chromatographic science 20050101 |
| Development of reactive thiol-modified monolithic capillaries and in-column surface functionalization by radical addition of a chromatographic ligand for capillary electrochromatography. | Journal of chromatography. A 20040730 |
| Enantiomer separation by countercurrent chromatography using cinchona alkaloid derivatives as chiral selectors. | Analytical chemistry 20020815 |
| Development of stereoselective nonaqueous capillary electrophoresis system for the resolution of cationic and amphoteric analytes. | Electrophoresis 20010901 |
| Supported liquid membrane stability in chiral resolution by chemically and physically modified membranes. | Annali di chimica 20010101 |
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