7499-04-9 Usage
Description
(1-hydroxycyclopentyl)acetic acid is a cyclopentane carboxylic acid derivative, characterized as a colorless liquid with the molecular formula C7H12O3 and a molecular weight of 144.17 g/mol. It is a versatile compound with applications in various fields, including organic synthesis, pharmaceuticals, and agrochemicals.
Uses
Used in Organic Synthesis:
(1-hydroxycyclopentyl)acetic acid serves as a key building block in the synthesis of complex organic molecules, facilitating the creation of a wide range of chemical compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (1-hydroxycyclopentyl)acetic acid is utilized for the preparation of various drugs, capitalizing on its anti-inflammatory and analgesic properties to develop new therapeutic agents.
Used in Agrochemical Industry:
(1-hydroxycyclopentyl)acetic acid also finds application in the agrochemical field, where it is employed in the development of pesticides and other agricultural chemicals to improve crop protection and yield.
Used in Neurological Research:
Furthermore, (1-hydroxycyclopentyl)acetic acid has been studied for its potential role in treating neurological disorders and neurodegenerative diseases, indicating its importance in advancing medical research and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 7499-04-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7499-04:
(6*7)+(5*4)+(4*9)+(3*9)+(2*0)+(1*4)=129
129 % 10 = 9
So 7499-04-9 is a valid CAS Registry Number.
7499-04-9Relevant articles and documents
BENZOIMIDAZOL-1,2-YL AMIDES AS Kv7 CHANNEL ACTIVATORS
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Paragraph 0259; 0261, (2016/04/09)
Optionally substituted benzoimidazol-1,2-yl amides, such as compounds of Formula 1 or Formula 2, can be used to treat disorders associated with a Kv7 potassium channel activator. Compositions, medicaments, and dosage forms related to the treatment are als
Synthesis of perhydrooxazinones from 2-aza-3-trimethylsilyloxy-1,3- butadiene. A general route to 3,3-disubstituted-β-hydroxy acids
Bandini, Elisa,Martelli, Giorgio,Spunta, Giuseppe,Bongini, Alessandro,Panunzio, Mauro
, p. 1735 - 1738 (2007/10/03)
1-Phenyl-2-aza-3-trimethylsilyloxy-1,3-butadiene reacts with aliphatic, aromatic and cyclic ketones to give in good to excellent yields 6,6- disubstituted-1,3-perhydro-oxazin-4-ones which, in turn, have been readily converted into β-hydroxy carboxylic acids.