1502-46-1 Usage
Uses
Used in Organic Chemistry:
2,5,8-Trihydroxy-1,3,4,6,7,9,9b-heptaaza-9bH-phenalene is used as a building block in organic chemistry for the synthesis of other complex compounds. Its structural complexity and functional groups make it a valuable intermediate in the preparation of various organic molecules.
Used in Molecular Design:
2,5,8-Trihydroxy-1,3,4,6,7,9,9b-heptaaza-9bH-phenalene is used as a component in designing intricate molecular systems, potentially for applications in materials science or nanotechnology. The presence of multiple hydroxy and aza groups allows for the formation of stable complexes and interactions with other molecules, contributing to the overall stability and functionality of the designed systems.
Used in Pharmaceutical Synthesis:
2,5,8-Trihydroxy-1,3,4,6,7,9,9b-heptaaza-9bH-phenalene is used as a precursor in the synthesis of pharmaceuticals. Its complex structure and functional groups may be exploited to create novel drug candidates with potential therapeutic applications. 2,5,8-Trihydroxy-1,3,4,6,7,9,9b-heptaaza-9bH-phenalene's ability to form stable complexes with other molecules could be particularly useful in the development of targeted drug delivery systems or in enhancing the bioavailability of certain drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 1502-46-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1502-46:
(6*1)+(5*5)+(4*0)+(3*2)+(2*4)+(1*6)=51
51 % 10 = 1
So 1502-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3N7O3/c14-4-7-1-8-5(15)10-3-12-6(16)11-2(9-4)13(1)3/h(H3,7,8,9,10,11,12,14,15,16)
1502-46-1Relevant academic research and scientific papers
Process for preparing cyameluric chloride
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Page/Page column 4, (2008/06/13)
The present invention concerns an improved process for obtaining larger quantities (several 10 grams up to kilograms) of pure cyameluric chloride (I) by chlorination of cyameluric acid (C6N7(OH)3) or its alkaline salts followed by fractioned vacuum sublimation.
