492-10-4 Usage
Description
2-amino-1,5-dihydro-7-methylpteridine-4,6-dione is a pteridine derivative with the molecular formula C8H8N4O2. It is a heterocyclic compound that features a pyrimidine ring fused to an imidazole ring. 2-amino-1,5-dihydro-7-methylpteridine-4,6-dione serves as a precursor in the biosynthesis of crucial molecules such as folates, which are vital for DNA synthesis and various metabolic processes.
Uses
Used in Pharmaceutical Production:
2-amino-1,5-dihydro-7-methylpteridine-4,6-dione is utilized as an intermediate in the synthesis of various pharmaceuticals. Its role in the production process is essential for creating medications that target different medical conditions.
Used in Laboratory Research:
As a component in laboratory research, 2-amino-1,5-dihydro-7-methylpteridine-4,6-dione contributes to the study and understanding of pteridine derivatives and their potential applications in medicine and biology.
Used in Drug Development:
2-amino-1,5-dihydro-7-methylpteridine-4,6-dione holds potential for the development of new drugs and therapies. Its involvement in the biosynthesis of important molecules like folates makes it a promising candidate for research into novel treatments for a variety of medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 492-10-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 492-10:
(5*4)+(4*9)+(3*2)+(2*1)+(1*0)=64
64 % 10 = 4
So 492-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N5O2/c1-2-5(13)10-3-4(9-2)11-7(8)12-6(3)14/h1H3,(H,10,13)(H3,8,9,11,12,14)
492-10-4Relevant articles and documents
One-step synthesis of lumazine and xanthine: First co-crystal of lumazine and perchloric acid with a unique monohydrated hydronium ion (H 5O2+) mediated supramolecular assembly of the lumazine dimer
Goswami, Shyamaprosad,Maity, Annada C.,Fun, Hoong-Kun
, p. 4056 - 4064 (2008/02/13)
A perchloric acid mediated one-step synthesis of lumazine derivatives from pterins and xanthine from guanine is reported. However, 2-pivaloylamino derivatives of pterins underwent simple hydrolysis of the pivaloylamino group generating free pterin compounds, but the 2-oxo derivatives, that is, the lumazine compounds, were not obtained. A novel supramolecular assembly is constructed by the unique hydrogen bonding of H5O2 + bridging two hydrogen-bonded dimers of lumazine to form the co-crystal 21 with aqueous perchloric acid. In contrast, N2-pivaloyl- 6-bromo-5-deazapterin was simply hydrolysed to form the protonated deazapterin 22, which forms a unique six-membered cyclic hydrogen-bonded structure leading to the generation of a polymeric supramolecular assembly. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
