74928-53-3

Upstream product

• 516-06-3 D,L-valine 
• 99-33-2 3,5-dinitrobenoyl chloride 

Downstream Products

• 126759-12-4 N-(3,5-dinitrobenzoyl)valine N-propylamide 

Relevant academic research and scientific papers

Thiourea Derivative of 2-[(1 R)-1-Aminoethyl]phenol: A Flexible Pocket-like Chiral Solvating Agent (CSA) for the Enantiodifferentiation of Amino Acid Derivatives by NMR Spectroscopy

Thiourea derivatives of 2-[(1R)-1-aminoethyl]phenol, (1S,2R)-1-amino-2,3-dihydro-1H-inden-2-ol, (1R,2R)-(1S,2R)-1-amino-2,3-dihydro-1H-inden-2-ol, and (R)-1-phenylethanamine have been compared as chiral solvating agents (CSAs) for the enantiodiscrimination of derivatized amino acids using nuclear magnetic resonance (NMR) spectroscopy. Thiourea derivative, prepared by reacting 2-[(1R)-1-aminoethyl]phenol with benzoyl isothiocyanate, constitutes an effective CSA for the enantiodiscrimination of N-3,5-dinitrobenzoyl (DNB) derivatives of amino acids with free or derivatized carboxyl functions. A base additive 1,4-diazabicyclo[2.2.2]octane(DABCO)/N,N-dimethylpyridin-4-amine (DMAP)/NBu4OH) is required both to solubilize amino acid derivatives with free carboxyl groups in CDCl3 and to mediate their interaction with the chiral auxiliary to attain efficient differentiation of the NMR signals of enantiomeric substrates. For ternary systems CSA/substrate/DABCO, the chiral discrimination mechanism has been ascertained through the NMR determination of complexation stoichiometry, association constants, and stereochemical features of the diastereomeric solvates.

Chiral mono- And dicarbamates derived from ethyl (: S)-lactate: convenient chiral solvating agents for the direct and efficient enantiodiscrimination of amino acid derivatives by 1H NMR spectroscopy

New chiral solvating agents (CSAs) for NMR spectroscopy have been obtained from ethyl (S)-lactate, a very cheap commercially available product. By a sequence of simple chemical modifications of its functional groups, monocarbamoylated and dicarbamoylated

Preparation of a New Chiral Stationary Phase Based on Macrocyclic Amide Chiral Selector for the Liquid Chromatographic Chiral Separations

A new chiral stationary phase (CSP) based on macrocyclic amide receptor was prepared starting from (1R,2R)-1,2-diphenylethylenediamine. The new CSP was successfully applied to the resolution of various N-(substituted benzoyl)-α-amino amides with reasonably good separation factors and resolutions (α = 1.75 ~ 2.97 and RS = 2.89 ~ 6.82 for 16 analytes). The new CSP was also applied to the resolution of 3-substituted 1,4-benzodiazepin-2-ones and some diuretic chiral drugs including bendroflumethiazide and methylchlothiazide and metolazone. The resolution results for 3-substituted 1,4-benzodiazepin-2-ones and some diuretic chiral drugs were also reasonably good. Chirality 28:253-258, 2016.

Synthesis, characterization and biological activity of Cu(II) chelates with some amino acid derivatives

The complexing behaviour of seventeen amino acid derivatives towards Cu(II) has been studied.Complexes of the types Cu(RH)*xH2O, Cu(RH).Cu(OH)2*xH2O and Cu(R'H)2*yH2O have been prepared and characterized by IR, ESR, electronic spectral, magnetic moment and analytical data.On the basis of differences and direction of the shifts in the IR frequencies of vas OCO and vs OCO modes and ESR spectra, bonding modes of carboxylate group have been established.Biological activitu of complexes is more than that of the free metal ion and the ligands.

A Chiral Stationary Phase for the Facile Resolution of Amino Acids, Amino Alcohols, and Amines as the N-3,5-Dinitrobenzoyl Derivatives

A chiral stationary phase derived from α-(6,7-dimethyl-1-naphthyl)isobutylamine is quite effective for the liquid chromatographic separation of the enantiomers of the N-3,5-dinitrobenzoyl derivatives of α-amino acids, their esters and amides, amino alcoho