2625-25-4 Usage
Uses
Used in Pharmaceutical Industry:
1,3,6,7-tetramethylpteridine-2,4(1H,3H)-dione is used as a therapeutic agent for the treatment of neurological and cardiovascular disorders. Its role in neurotransmitter synthesis and nitric oxide production makes it a potential candidate for managing conditions such as phenylketonuria and hypertension.
Used in Neurotransmitter Synthesis:
1,3,6,7-tetramethylpteridine-2,4(1H,3H)-dione is used as a co-factor in the synthesis of neurotransmitters like serotonin, dopamine, and norepinephrine, which are essential for various physiological processes, including mood regulation, cognitive function, and motor control.
Used in Nitric Oxide Production:
1,3,6,7-tetramethylpteridine-2,4(1H,3H)-dione is used as a critical component in the production of nitric oxide, a molecule that plays a significant role in maintaining cardiovascular health by regulating blood vessel dilation and preventing platelet aggregation.
Used in Research and Development:
1,3,6,7-tetramethylpteridine-2,4(1H,3H)-dione is used as a subject of research to better understand its role in various biological processes and to develop new therapeutic strategies for treating neurological and cardiovascular disorders associated with BH4 deficiencies.
Check Digit Verification of cas no
The CAS Registry Mumber 2625-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2625-25:
(6*2)+(5*6)+(4*2)+(3*5)+(2*2)+(1*5)=74
74 % 10 = 4
So 2625-25-4 is a valid CAS Registry Number.
2625-25-4Relevant academic research and scientific papers
Reaction of Pyrazine-2,3-dicarbonitrile and 1,3-Dimethyllumazine with the Phthalimidoalkyl Radical
Tada, Masaru,Totoki, Shintaro
, p. 1295 - 1299 (2007/10/02)
A phthalimidoalkyl radical reacts with pyrazine-2,3-dicarbonitrile (1) to give mono- and diphthalimidoalkylpyrazine-2,3-dicarbonitriles 4 and 5.Similar reaction with 1,3-dimethyllumazine (2) gave only monophthalimidoalkyl-1,3-dimethyllumazines 6 or 7.Hydrazine degradation of 7-(3'-phthalimido)propyl-1,3-dimethyllumazine (6c) gave a 7-(3'-amino)propyl derivative 8 but 7-phthalimidomethyl-1,3-dimethyllumazine (6a) gave only 1,3-dimethyllumazine (2).Thus the phthalimidomethyl group can be used as a protection group of the pteridine nucleus.
