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The chemical compound "[6-(4-Fluoro-2-methyl-benzoyl)-1,4-di-pyridin-3-yl-1,4-dihydro-[1,2,4,5]tetrazin-3-yl]-(4-fluoro-2-methyl-phenyl)-methanone" is a complex organic molecule with a molecular formula of C23H16F2N6O. It features a tetrazin-3-yl core, which is a heterocyclic ring system containing four nitrogen atoms. The compound is characterized by the presence of two pyridin-3-yl groups, which are pyridine rings with a nitrogen atom at the 3-position. Additionally, it has a 4-fluoro-2-methyl-benzoyl group attached to the tetrazin-3-yl core, which contributes to its structure and potential properties. The compound also includes a 4-fluoro-2-methyl-phenyl group, which is a phenyl ring with a fluorine atom at the 4-position and a methyl group at the 2-position. This chemical is likely to be of interest in the fields of medicinal chemistry and materials science due to its unique structure and potential applications in drug development or as a building block for more complex molecules.

78938-20-2

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78938-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78938-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,3 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78938-20:
(7*7)+(6*8)+(5*9)+(4*3)+(3*8)+(2*2)+(1*0)=182
182 % 10 = 2
So 78938-20-2 is a valid CAS Registry Number.

78938-20-2Downstream Products

78938-20-2Relevant academic research and scientific papers

Reaction of N-Phenacyl- or Substituted Phenacyl-pyridinium Bromide with 3-Pyridyldiazonium Chloride - Synthesis of a New Series of 1,4-Dihydro-1,2,4,5-tetrazines through Pyridinium Ylid

Bansal, R. K.,Bhagchandani, Gope

, p. 503 - 504 (2007/10/02)

The reaction of N-phenacyl- or substituted phenacyl-pyridinium bromide with 3-pyridyldiazonium chloride obtained from 3-aminopyridine, furnishes the corresponding 1,4-dihydro-1,2,4,5-tetrazines.Their structures are supported by elemental analyses, IR and PMR spectra.

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