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L-glutamic acid dianilide, also known as L-glutamate dianilide or L-Glutamic acid 5-(4-aminophenyl)-5-oxo-L-prolinamide, is a synthetic chemical compound with the molecular formula C16H18N2O4. It is derived from the combination of L-glutamic acid, an amino acid, and anilide, a derivative of aniline. L-glutamic acid dianilide is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various drugs, particularly those targeting the central nervous system. Its structure allows for the modulation of neurotransmitter activity, making it a valuable component in the development of medications for conditions such as Parkinson's disease, schizophrenia, and other neurological disorders.

2643-65-4

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2643-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2643-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2643-65:
(6*2)+(5*6)+(4*4)+(3*3)+(2*6)+(1*5)=84
84 % 10 = 4
So 2643-65-4 is a valid CAS Registry Number.

2643-65-4Relevant academic research and scientific papers

Development of a new class of chiral phosphorus ligands: P-chirogenic diaminophosphine oxides. A unique source of enantioselection in Pd-catalyzed asymmetric construction of quaternary carbons

Nemoto, Tetsuhiro,Masuda, Takamasa,Matsumoto, Takayoshi,Hamada, Yasumasa

, p. 7172 - 7178 (2007/10/03)

We have recently developed a new class of chiral phosphorus ligands: P-chirogenic diaminophosphine oxides. These pentavalent phosphorus compounds have been successfully applied to Pd-catalyzed asymmetric construction of tertiary and quaternary carbons. The actual ligand structure was the trivalent phosphorus species 17, which was generated in situ by BSA-induced P(V) to P(III) transformation of 6, the preligand. Detailed mechanistic studies, including asymmetric amplification and initial rate kinetics, revealed that complex 18 [Pd-17 (1:2) complex] was the active catalyst. The important function of the nitrogen atom on the sidearm in the ligands was also clarified. The source of enantioselection in the construction of asymmetric quaternary carbons was the secondary ligand substrate interaction mediated by N-Zn coordination.

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