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N-methyl-N-phenyl-N'-(2-(3-methylpyridine))formamidine is a complex organic compound with the molecular formula C15H16N4. It is a derivative of formamidines, which are characterized by the presence of a formamidine group (-NH-NH2). This particular compound features a methyl group (-CH3) attached to the nitrogen atom, a phenyl group (C6H5), and a 3-methylpyridine moiety, which is a pyridine ring with a methyl group at the 3rd position. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving formamidine and the appropriate aromatic or heterocyclic components. The compound's properties, such as solubility and stability, can vary depending on the specific conditions under which it is prepared and stored.

3189-06-8

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3189-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3189-06-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3189-06:
(6*3)+(5*1)+(4*8)+(3*9)+(2*0)+(1*6)=88
88 % 10 = 8
So 3189-06-8 is a valid CAS Registry Number.

3189-06-8Downstream Products

3189-06-8Relevant academic research and scientific papers

Preparation method for 7-azaindole

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Paragraph 0022-0030, (2019/01/08)

The invention discloses a preparation method for 7-azaindole, and belongs to technical field of the medicinal chemistry synthesis. The preparation method comprises the following steps: using a compound I, namely 2-amino-3-methylpyridine and N-methylformanilide, to perform an addition elimination reaction under the action of a dehydrating agent, to obtain a compound II; performing intramolecular ring closure on the compound II under the action of strong base, to obtain a target compound III. The preparation method is capable of acquiring the target product through two-step synthesis only. The method is simple in post-treatment, less in side reaction, high in yield, and in comply with requirements of industrial production. (The formula is shown in the description.).

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