1236-39-1 Usage
Molecular Structure
The compound has a complex molecular structure that contains a naphthalen-2-yl group attached to an isoquinolinium moiety.
Functional Groups
It features a hydroxy and two dioxo groups in the naphthalen-2-yl portion, which may contribute to its biological and pharmacological activity.
Potential Applications
Due to its unique structure and potential reactivity, 2-(1-hydroxy-3,4-dioxo-3,4-dihydronaphthalen-2-yl)isoquinolinium may have applications in medicinal chemistry, biochemistry, and drug development.
Ongoing Research
Research into the properties and potential uses of 2-(1-hydroxy-3,4-dioxo-3,4-dihydronaphthalen-2-yl)isoquinolinium is ongoing, and it may hold promise for future therapeutic or scientific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1236-39-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1236-39:
(6*1)+(5*2)+(4*3)+(3*6)+(2*3)+(1*9)=61
61 % 10 = 1
So 1236-39-1 is a valid CAS Registry Number.
1236-39-1Relevant articles and documents
Synthesis of 2-oxy-3-(pyridinium-1'-yl)-l,4-naphthoquinone derivatives by iodine or hydrogen peroxide oxidation of 1,4-naphthoquinones in the presence of substituted pyridines
Citterio, Attilio,Fochi, Mariacristina,Maronati, Antonietta,Sebastiano, Roberto,Mele, Andrea
, p. 614 - 616 (1997)
2-Oxy-3-(pyridinium-1'-yl)-1.4-naphthoquinone betaines are obtained in moderate to good yield by oxidation of 1,4-naphthoquinones with iodine MnO2 or hydrogen peroxide in the presence of substituted pyridines. Pyridinium- 1,4-naphthoquinone iodides and 2.3-epoxy-2.3-dihydronaphthoquinone are suggested intermediates.
