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3-phenylphthalazin-3-ium-1-olate is an organic compound with the molecular formula C16H11NO. It is a derivative of phthalazine, a heterocyclic aromatic compound consisting of two fused six-membered rings, one of which is a nitrogen-containing pyrazine ring. The 3-phenyl group in 3-phenylphthalazin-3-ium-1-olate is attached to the phthalazine core, which significantly influences its chemical and physical properties. 3-phenylphthalazin-3-ium-1-olate is known for its potential applications in various fields, such as pharmaceuticals, dyes, and materials science, due to its unique structure and reactivity. It can be synthesized through various chemical reactions, and its properties can be further modified by introducing different functional groups or substituents. Overall, 3-phenylphthalazin-3-ium-1-olate is an intriguing chemical entity with a wide range of potential applications and areas for further research and development.

4870-18-2

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4870-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4870-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4870-18:
(6*4)+(5*8)+(4*7)+(3*0)+(2*1)+(1*8)=102
102 % 10 = 2
So 4870-18-2 is a valid CAS Registry Number.

4870-18-2Downstream Products

4870-18-2Relevant academic research and scientific papers

Gram-scale production of nitrogen doped graphene using a 1,3-dipolar organic precursor and its utilisation as a stable, metal free oxygen evolution reaction catalyst

Bayazit, Mustafa K.,Moniz, Savio J. A.,Coleman, Karl S.

supporting information, p. 7748 - 7751 (2017/07/15)

For the first time, a one-step scalable synthesis of a few-layer ～10% nitrogen doped (N-doped) graphene nanosheets (GNSs) from a stable but highly reactive 1,3-dipolar organic precursor is reported. The utilization of these N-doped GNSs as metal-free electrocatalysts for the oxygen evolution reaction (OER) is also demonstrated. This process may open the path for the scalable production of other heteroatom doped GNSs by using the broad library of well-known, stable 1,3-dipolar organic compounds.

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