26109-19-3 Usage
Uses
Used in Organic Synthesis:
(S)-2-Fluorosuccinic acid is utilized as a key building block in organic synthesis, contributing to the development of various chemical compounds and materials.
Used in Pharmaceutical Production:
As a crucial component in the production of pharmaceuticals, (S)-2-Fluorosuccinic acid aids in the creation of medications that target a range of health conditions.
Used in Agrochemicals:
(S)-2-Fluorosuccinic acid is also employed in the production of agrochemicals, which are chemicals used in the agricultural industry to enhance crop protection and yield.
Used in Medicinal Chemistry Research:
(S)-2-Fluorosuccinic acid is investigated for its potential anti-tumor properties, making it a valuable molecule in the quest for novel cancer treatments.
Used in Pharmaceutical Research:
(S)-2-Fluorosuccinic acid's anti-inflammatory activities are being studied, which could lead to the development of new therapies for inflammatory diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 26109-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,0 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26109-19:
(7*2)+(6*6)+(5*1)+(4*0)+(3*9)+(2*1)+(1*9)=93
93 % 10 = 3
So 26109-19-3 is a valid CAS Registry Number.
26109-19-3Relevant academic research and scientific papers
Synthesis, Absolute Configuration, and Circular Dichroism of the Enantiomers of Fluorosuccinic Acid
Lowe, Gordon,Potter, Barry V. L.
, p. 2029 - 2032 (2007/10/02)
Diethylaminosulphur trifluoride (DAST) converts (2S)- and (2R)-malate esters into the enantiomeric fluorosuccinate esters. (2S,3R)-Malate, obtained from fumarate by fumarase-catalysed hydration in deuterium oxide, was used to show that the reaction with DAST occurs stereospecifically with inversion of configuration.Conversion of (2S)-aspartic acid into fluorosuccinate with sodium nitrite in polyhydrogen fluoride-pyridine occurs predominantly with retention of configuration.The circular dichroic spectra of (2S)- and (2R)-fluorosuccinic acids and their methyl esters are 'anomalous' and consequently the absolute configuration previously assigned to a Pseudomonal metabolite, (+)-fluorosuccinic acid, is shown to be erroneous.
