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3-methoxy-N-[(7-methyltetrazolo[1,5-a]quinolin-4-yl)methyl]-N-(pyridin-3-ylmethyl)benzamide is a complex organic compound with a molecular formula of C23H20N6O2. It is characterized by a benzamide core, which is substituted with a 3-methoxy group and two-m Nethyl groups attached to a pyridin-3-yl and a 7-methyltetrazolo[1,5-a]quinolin-4-yl moiety, respectively. 3-methoxy-N-[(7-methyltetrazolo[1,5-a]quinolin-4-yl)methyl]-N-(pyridin-3-ylmethyl)benzamide is of interest in medicinal chemistry due to its potential as a biologically active molecule, possibly serving as a precursor or intermediate in the synthesis of pharmaceuticals. Its structure suggests that it may have applications in the development of drugs targeting various receptors or enzymes, given the presence of multiple heterocycles and functional groups that can interact with biological targets.

5192-02-9

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5192-02-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5192-02-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,9 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5192-02:
(6*5)+(5*1)+(4*9)+(3*2)+(2*0)+(1*2)=79
79 % 10 = 9
So 5192-02-9 is a valid CAS Registry Number.

5192-02-9Downstream Products

5192-02-9Relevant academic research and scientific papers

Practical synthesis of optically pure methyl (2R,3S)-2,3-epoxybutanoate via microbial asymmetric reduction of α-chloroacetoacetate

Akita,Todoroki,Endo,Ikari,Oishi

, p. 513 - 516 (2007/10/02)

Asymmetric reduction of ethyl α-chloroacetoacetate (3) with Baker's yeast followed by treatment with sodium ethoxide afforded a mixture of ethyl (2R,3S)-(8) and (2S,3S)-2,3-epoxybutanoate (9) (8/9, 85:15), which could be converted into the optically pure methyl (2R,3S)-2,3-epoxybutanoate (25) via one recrystallization of the brucine salt of the diastereomeric mixture of the corresponding epoxy acid.

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