29639-68-7 Usage
Uses
Used in Pharmaceutical Synthesis:
4,6-Dihydroxy-2-methythiopyrimidine is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various drug molecules, enhancing their therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 4,6-Dihydroxy-2-methythiopyrimidine is utilized as a building block in the creation of compounds that have pesticidal or herbicidal properties, contributing to crop protection and yield enhancement.
Used as an Anti-bacterial Agent:
4,6-Dihydroxy-2-methythiopyrimidine is used as an anti-bacterial agent for its potential to combat bacterial infections, making it a candidate for development in the field of antimicrobial chemotherapy.
Used as an Anti-fungal Agent:
Similarly, it is used as an anti-fungal agent, indicating its broad-spectrum activity against fungi, which is valuable in both medical and agricultural applications for controlling fungal diseases.
Used for Antioxidant Properties:
4,6-Dihydroxy-2-methythiopyrimidine is used to leverage its antioxidant properties, which can be beneficial in the development of treatments aimed at combating oxidative stress-related conditions.
Used for Neuroprotective Applications:
Its neuroprotective properties make 4,6-Dihydroxy-2-methythiopyrimidine a candidate for use in neurodegenerative disease research and therapeutics, potentially protecting neurons from damage and degeneration.
Check Digit Verification of cas no
The CAS Registry Mumber 29639-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,3 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29639-68:
(7*2)+(6*9)+(5*6)+(4*3)+(3*9)+(2*6)+(1*8)=157
157 % 10 = 7
So 29639-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2S/c1-10-5-6-3(8)2-4(9)7-5/h2H2,1H3,(H,6,7,8,9)
29639-68-7Relevant academic research and scientific papers
Reaction of Thiobarbituric Acid and Hydrazine: Formation of a Secondary Amine
Pradhan, P. C.,Mishra, B. K.,Behera, G. B.
, p. 1097 - 1098 (2007/10/02)
Reaction of 2-methylmercaptobarbituric acid (2) with hydrazine leads to a secondary amine, 2,2-bis(3,4,5,6-tetrahydropyrimidyl)amine (4) instead of s-trihydrazinopyrimidine.A plausible mechanism is proposed for the formation of 4.
