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6-Methyl-4H-indolo[3,2,1-de][1,5]naphthyridin-4-one is an alkaloid compound that has been isolated from the yellow stem bark of Pleiocarpa mutica Benth. It crystallizes as long yellow needles from MeOH and exhibits unique absorption maxima in its ultraviolet spectrum. 6-Methyl-4H-indolo[3,2,1-de][1,5]naphthyridin-4-one can undergo hydrogenation in the presence of Pd to yield an amorphous tetrahydro derivative, which can further react with AC20 in pyridine to form an acetyltetrahydro compound, also amorphous.

3464-65-1

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3464-65-1 Usage

Uses

Used in Pharmaceutical Industry:
6-Methyl-4H-indolo[3,2,1-de][1,5]naphthyridin-4-one is used as a pharmaceutical compound for its potential therapeutic applications. 6-Methyl-4H-indolo[3,2,1-de][1,5]naphthyridin-4-one's unique chemical structure and properties make it a promising candidate for the development of new drugs targeting various diseases and conditions.
Used in Chemical Research:
In the field of chemical research, 6-Methyl-4H-indolo[3,2,1-de][1,5]naphthyridin-4-one serves as a valuable subject for studying its chemical properties, reactivity, and potential applications in the synthesis of other compounds. Its hydrogenation and acetylation reactions provide insights into the compound's behavior under different conditions, which can be useful for designing new synthetic routes and understanding its potential applications.
Used in Drug Synthesis:
6-Methyl-4H-indolo[3,2,1-de][1,5]naphthyridin-4-one can be used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs with improved efficacy and selectivity.
Used in Material Science:
6-Methyl-4H-indolo[3,2,1-de][1,5]naphthyridin-4-one's amorphous nature and unique optical properties make it a potential candidate for applications in material science, such as in the development of new materials with specific optical, electronic, or mechanical properties.

References

Achenbach, Biemann., 1. Amer. Chem. Soc., 87,4177 (1965)

Check Digit Verification of cas no

The CAS Registry Mumber 3464-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3464-65:
(6*3)+(5*4)+(4*6)+(3*4)+(2*6)+(1*5)=91
91 % 10 = 1
So 3464-65-1 is a valid CAS Registry Number.

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