583031-57-6 Usage
General Description
1,8-Naphthyridin-2(1H)-one, 4-chloro-1-(phenylmethyl)- is a chemical compound with a naphthyridine structure, chloro and phenylmethyl functional groups. It is also known as Zolpidem, a sedative and hypnotic medication primarily used for the treatment of insomnia. Zolpidem works by enhancing the effect of neurotransmitter gamma-aminobutyric acid (GABA) in the brain, leading to a calming effect and improved sleep. It is available in various formulations such as immediate-release tablets, extended-release tablets, and oral spray, and is typically prescribed for short-term use. However, it is important to use Zolpidem cautiously and under medical supervision due to the potential for dependence, tolerance, and withdrawal symptoms with prolonged use.
Check Digit Verification of cas no
The CAS Registry Mumber 583031-57-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,3,0,3 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 583031-57:
(8*5)+(7*8)+(6*3)+(5*0)+(4*3)+(3*1)+(2*5)+(1*7)=146
146 % 10 = 6
So 583031-57-6 is a valid CAS Registry Number.
583031-57-6Relevant articles and documents
4-thio substituted quinoline and naphthyridine compounds
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Page/Page column 18, (2009/04/24)
The present invention relates to 4-thio substituted quinoline and naphthyridine derivatives and processes for their preparation. The invention also related to methods for treating infection of Hepatitis C virus by administering a 4-thio substituted quinoline or naphthyridine derivative.
Synthesis of SMP-797: A new potent ACAT inhibitor
Ban, Hitoshi,Muraoka, Masami,Ohashi, Naohito
, p. 10081 - 10092 (2007/10/03)
A potent ACAT (acyl-CoA: cholesterol acyltransferase) inhibitor SMP-797 was effectively synthesized by the urea formation of 3-amino-4-aryl-1,8- naphthyridin-2(1H)-one and 4-amino-2,6-diisopropylamine. The synthesis of the former compound involved the Suzuki coupling reaction as a key step, and the latter was prepared by the 4-selective nitration of 2,6-diisopropylaniline using 2,3,5,6-tetrabromo-4-methyl-4-nitro-2,5-cyclohexadienone.
