117835-08-2 Usage
Uses
Used in Pharmaceutical Synthesis:
5-PHENYL-2,4-PYRROLIDINEDICARBOXYLIC ACID is used as an intermediate in the production of drugs for its ability to form essential molecular structures. Its unique properties contribute to the development of new and effective pharmaceutical compounds.
Used in Organic Chemistry:
In the field of organic chemistry, 5-PHENYL-2,4-PYRROLIDINEDICARBOXYLIC ACID is used as a building block for the synthesis of complex organic molecules. Its reactivity and structural features enable the creation of a wide range of chemical products.
Used as a Chelating Agent in Metal Ion Extraction:
5-PHENYL-2,4-PYRROLIDINEDICARBOXYLIC ACID is utilized as a chelating agent in the extraction of metal ions. Its ability to form stable complexes with metal ions makes it an effective tool in various industrial processes, including environmental remediation and material science.
Used in Chemical Processes:
Due to its unique structure and properties, 5-PHENYL-2,4-PYRROLIDINEDICARBOXYLIC ACID is employed in a variety of chemical processes. It can act as a catalyst, a reagent, or a precursor in the synthesis of various compounds, contributing to the advancement of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 117835-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,3 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 117835-08:
(8*1)+(7*1)+(6*7)+(5*8)+(4*3)+(3*5)+(2*0)+(1*8)=132
132 % 10 = 2
So 117835-08-2 is a valid CAS Registry Number.
117835-08-2Relevant academic research and scientific papers
FAST ATOM BOMBARDMENT (FAB) AND CHEMICAL IONIZATION (CI) MASS SPECTROMETRY OF Γ-CARBOXYGLUTAMIC ACID, 5-SUBSTITUTED-4,4-DICARBOXYPROLINES, AND THEIR MONODECARBOXY DERIVATIVES GLUTAMIC ACID AND 5-SUBSTITUTED-4-CARBOXYPROLINES
Capasso, R.,Pucci, P.,Randazzo, G.,Malorni, A.
, p. 2177 - 2180 (2007/10/02)
DL-Carboxyglutamic acid (Gla) reacts easily and quantitatively with aldehydes to give the racemic diastereoisomers of 5-substituted-4,4-dicarboxyprolines.After heating at 100 deg C for 30 minutes these amino acids lose a carboxyl group from C-γ of Gla and C-4 of the proline ring to give glutamic acid and the racemic diastereoisomers of cyclic analogs of glutamic acid respectively.This paper reports a study of the above-mentioned compounds by using FAB mass spectrometry in comparison with CI analysis.FAB turned out to be an adequate ionization technique for dealing with such nonvolatile and thermolabile amino acids, and may thus allow the development of a rapid and sensitive method for detecting γ-carboxyglutamic acid urine and in other biological matrices in pathological cases (i.e., renal stones and blood serum).
