1198098-52-0 Usage
Uses
Used in Pharmaceutical Industry:
(E)-5-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde oxime is used as a building block for the synthesis of potential drug candidates due to its versatile reactivity and significant chemical and biological properties. Its unique structure and properties make it a promising candidate for the development of new pharmaceuticals.
Used in Materials Science:
In the field of materials science, (E)-5-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde oxime is used in the design of organic semiconductors and electronic materials. Its unique properties and reactivity contribute to the development of advanced materials with potential applications in various electronic devices and technologies.
Overall, (E)-5-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde oxime is a versatile and valuable compound in the realms of organic chemistry and material science, with a wide range of applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1198098-52-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,0,9 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1198098-52:
(9*1)+(8*1)+(7*9)+(6*8)+(5*0)+(4*9)+(3*8)+(2*5)+(1*2)=200
200 % 10 = 0
So 1198098-52-0 is a valid CAS Registry Number.
1198098-52-0Relevant academic research and scientific papers
Synthesizing method of (E)-5-methyl-1H-pyrrolo-[2,3-b] pyridine-3-formaldoxime
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Paragraph 0008, (2017/09/02)
The invention relates to a synthesizing method of (E)-5-methyl-1H-pyrrolo-[2,3-b] pyridine-3-formaldoxime, which solves the technical problem that an effective synthesizing method is not discovered at present. The synthesizing method provided by the invention comprises the following steps: brominating 2-amino-5-picoline, so as to obtain a compound 1; performing a reaction on the compound 1 and trimethylsilylacetylene under a condition of a Sonogashira coupling reaction, so as to generate a compound 2; performing a reaction on the compound 2 and sodium hydride to form a pyrrole ring, so as to generate a compound 3; performing a reaction on the compound 3 and urotropine, so as to generate a compound 4; performing the compound 4, hydroxylamine hydrochloride and sodium acetate, so as to obtain the target product (E)-5-methyl-1H-pyrrolo-[2,3-b] pyridine-3-formaldoxime. As a sodium acetate, the (E)-5-methyl-1H-pyrrolo-[2,3-b] pyridine-3-formaldoxime is widely applied in the pharmaceutical industry.