1655-48-7 Usage
Description
DNP-DL-GLUTAMIC ACID is a chemical compound that results from the combination of 2,4-dinitrophenol (DNP) and DL-glutamic acid, a naturally occurring amino acid. This crystalline substance has potential pharmaceutical applications and may serve as a research tool in chemistry and biochemistry.
Uses
Used in Pharmaceutical Applications:
DNP-DL-GLUTAMIC ACID is used as a potential treatment for neurodegenerative diseases, given its unique structure and properties that could be harnessed for therapeutic purposes.
Used in Drug Synthesis:
DNP-DL-GLUTAMIC ACID is utilized in the synthesis of certain drugs and pharmaceuticals, contributing to the development of new medications and therapies.
Used in Chemical and Biochemical Research:
DNP-DL-GLUTAMIC ACID serves as a research tool in the fields of chemistry and biochemistry, aiding scientists in understanding complex biological processes and chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 1655-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1655-48:
(6*1)+(5*6)+(4*5)+(3*5)+(2*4)+(1*8)=87
87 % 10 = 7
So 1655-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H11N3O8/c15-10(16)4-3-8(11(17)18)12-7-2-1-6(13(19)20)5-9(7)14(21)22/h1-2,5,8,12H,3-4H2,(H,15,16)(H,17,18)
1655-48-7Relevant articles and documents
Kinetic study and analytical application of the hexadecyltrimethylammonium bromide-catalyzed reaction of 1-fluoro-2,4-dinitrobenzene with amines
Wong,Connors
, p. 146 - 150 (2007/10/02)
Arylation of amines by reaction with 1-fluoro-2,4-dinitrobenzene is catalyzed by micelles of cetrimonium bromide. This catalysis has been exploited to reduce the analysis time in the spectrophotometric determination of amines as their dinitrophenyl derivatives. The kinetics of the catalysis were studied for the five amines: alanine, phenylalanine, aniline, 4-methylaniline, and 4-methoxyaniline. The dependence of rate constant on surfactant concentration can be quantitatively accounted for by Berezin's model, in which uptake of the amine and the 1-fluoro-2,4-dinitrobenzene by the micelle is described as a partitioning phenomenon for both species. An alternative model is developed in which one reactant partitions into the micellar phase and the other binds to the micelle with 1:1 stoichiometry; the two models are formally equivalent. Intrinsic catalytic rate constants and binding constants were evaluated. About one-third to one-half of the maximum observed micellar acceleration is attributed to a true micellar catalysis, the remainder being ascribed to an increase in local reactant concentrations in the micelle.
