958334-24-2 Usage
Uses
Used in Organic Synthesis:
Methyl 7-bromo-1,5-naphthyridine-3-carboxylate is used as a building block in organic synthesis for the creation of various bioactive compounds. Its unique structure and bromine substituent allow for a wide range of chemical transformations, making it a valuable component in the synthesis of pharmaceuticals and other organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, methyl 7-bromo-1,5-naphthyridine-3-carboxylate is utilized as a key intermediate in the development of new drugs. Its potential applications include the synthesis of compounds with antimicrobial, antiviral, and anticancer properties. The bromine atom in its structure also makes it a candidate for cross-coupling reactions, which are essential in the formation of complex molecular structures.
Used in Materials Science:
Methyl 7-bromo-1,5-naphthyridine-3-carboxylate's versatility extends to the field of materials science, where it can be employed in the design and synthesis of novel materials with specific properties. Its unique chemical structure allows for the development of materials with potential applications in various industries, such as electronics, coatings, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 958334-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,3,3 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 958334-24:
(8*9)+(7*5)+(6*8)+(5*3)+(4*3)+(3*4)+(2*2)+(1*4)=202
202 % 10 = 2
So 958334-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H7BrN2O2/c1-15-10(14)6-2-8-9(12-4-6)3-7(11)5-13-8/h2-5H,1H3
958334-24-2Relevant academic research and scientific papers
Synthetic method of 7-bromo-1,5-naphthyridine-3-methanoic acid
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Paragraph 0063; 0064; 0065, (2018/11/03)
The invention provides a synthetic method of 7-bromo-1,5-naphthyridine-3-methanoic acid. The synthetic method of the 2-bromo-1,5-naphthyridine-3-methanoic acid comprises the steps of taking 1,5-naphthyridine as a raw material and reacting to generate 7-bromo-1,5-naphthyridine-3-methyl pyrazinecarboxylate; and finally hydrolyzing the 7-bromo-1,5-naphthyridine-3-methyl pyrazinecarboxylate under thealkaline condition to generate the 7-bromo-1,5-naphthyridine-3-methanoic acid. According to the synthetic method of the 7-bromo-1,5-naphthyridine-3-methanoic acid, a synthetic route which takes 1,5-naphthyridine as a raw material is provided. The synthetic method of the 7-bromo-1,5-naphthyridine-3-methanoic acid has the advantages that the synthetic route is simple, the raw materials are low in cost, are simple and are easily obtained, aftertreatment is facilitated, the success rate is high, the synthetic route is easy to enlarge and the like.
