1578-67-2 Usage
General Description
2-Fluoroglutaric acid is a chemical compound with the molecular formula C5H7FO4. It is a derivative of glutaric acid and contains a fluorine atom in the 2-position of the molecule. 2-Fluoroglutaric acid is used in the pharmaceutical industry as a building block for the synthesis of various drugs and pharmaceuticals. It has also been studied for its potential therapeutic applications in treating neurodegenerative diseases and certain metabolic disorders. 2-Fluoroglutaric acid is known to exhibit moderate toxicity and should be handled with care in laboratory and industrial settings. It is important to follow proper safety precautions and handling guidelines when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 1578-67-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1578-67:
(6*1)+(5*5)+(4*7)+(3*8)+(2*6)+(1*7)=102
102 % 10 = 2
So 1578-67-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H7FO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2H2,(H,7,8)(H,9,10)
1578-67-2Relevant articles and documents
Chemistry of Novel Compounds with Multifunctional Carbon Structure. 5. Molecular Design of Versatile Building Blocks for Aliphatic Monofluoro Molecules by Manipulation of Multifunctional Carbon Structure
Takeuchi, Yoshio,Nagata, Kazuhiro,Koizumi, Toru
, p. 5453 - 5459 (2007/10/02)
Three kinds of doubly functionalized monofluoromethylene fragments, 1-fluoro-1-nitro-1-(phenylsulfonyl)alkanes (10), 2-fluoro-2-(phenylsulfonyl)alkanoic esters (11), and 2-fluoro-2-nitroalkanoic esters (12), potentially versatile building blocks for the general synthesis of various aliphatic monofluoro molecules, were prepared from the corresponding difunctional compounds 1-3 by monoalkylation (R) and selective fluorinations.The interconversion or reductive removal of each functional group in 10-12 followed by the introduction of the second alkyl groups (R') at the fluorine-bearing carbon atom was examined.Compounds 12 proved to be useful and practical building blocks for conversions to the various monofluoroalkanes 20-26.
