32806-62-5 Usage
Uses
Used in Pharmaceutical Industry:
2-PROPYL GLUTARIC ACID is used as an intermediate compound for the synthesis of various pharmaceutical products. Its role in the metabolism of Valproic Acid makes it a valuable component in the development of new medications, particularly those targeting neurological and psychiatric disorders.
Used in Chemical Research:
As a white solid with distinct chemical properties, 2-PROPYL GLUTARIC ACID is utilized in chemical research for the investigation of its potential applications and interactions with other compounds. This research can lead to the discovery of new uses and benefits of the compound in various industries.
Used in Metabolism Studies:
2-PROPYL GLUTARIC ACID is used as a subject of study in the field of metabolism, particularly in understanding the metabolic pathways of Valproic Acid. This knowledge can contribute to the development of more effective treatments and therapies for conditions that respond to Valproic Acid.
Check Digit Verification of cas no
The CAS Registry Mumber 32806-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,0 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32806-62:
(7*3)+(6*2)+(5*8)+(4*0)+(3*6)+(2*6)+(1*2)=105
105 % 10 = 5
So 32806-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O4/c1-2-3-6(8(11)12)4-5-7(9)10/h6H,2-5H2,1H3,(H,9,10)(H,11,12)
32806-62-5Relevant academic research and scientific papers
Chain-extension Reactions of Acetylenes. Part 4. Reaction of 1,3-Dilithioacetylides with Carbonyl Electrophiles, Hexamethylphosphoric Triamide, and Benzylideneaniline
Pover, Keith A.,Scheinmann, Feodor
, p. 2338 - 2345 (2007/10/02)
The regioselectivity of the reactions of 1,3-dilithioalk-1-ynes with various electrophiles has been examined.With formaldehyde and cyclic ketones, reaction occur at C-1 and C-3 to give alk-2-yne-1,5-diols.In contrast reactions with carbon dioxide give allene-1,3-dicarboxylic acids. 1,3-Dilithioalk-1-ynes decompose hexamethylphosphoric triamide and the resulting N-methylmethyleneamine undergoes addition only at the propargylic site.Further reaction with either 1-bromobutane or water gives alkynylamines.Benzylideneaniline also reacts with 1,3-dilithiohex- and hept-1-ynes only at the propargylic site to give N-phenylbut-3-ynylamines.
