73576-32-6 Usage
Uses
Used in Pharmaceutical Industry:
2-Amino-4-hydroxy-6-isopropylpyrimidine is used as a building block for the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties.
Used in Cancer Therapy:
2-Amino-4-hydroxy-6-isopropylpyrimidine is used as an anti-cancer agent for its potential role in cancer treatment, targeting and inhibiting the growth of cancer cells.
Used in Neurological Disorder Treatment:
2-Amino-4-hydroxy-6-isopropylpyrimidine is used as a potential therapeutic agent for neurological disorders, given its potential to modulate specific biological pathways and mechanisms involved in these conditions.
Used in Antiviral Applications:
2-Amino-4-hydroxy-6-isopropylpyrimidine is used as an antiviral agent, leveraging its properties to inhibit viral replication and reduce the severity of viral infections.
Check Digit Verification of cas no
The CAS Registry Mumber 73576-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,7 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73576-32:
(7*7)+(6*3)+(5*5)+(4*7)+(3*6)+(2*3)+(1*2)=146
146 % 10 = 6
So 73576-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H11N3O/c1-4(2)5-3-6(11)10-7(8)9-5/h3-4H,1-2H3,(H3,8,9,10,11)
73576-32-6Relevant academic research and scientific papers
Direct synthesis of 5- and 6-substituted 2-aminopyrimidines as potential non-natural nucleobase analogues
Radhakrishnan,Sharma, Namita,Kundu, Lal Mohan
, p. 15087 - 15090 (2014/04/17)
A series of 2-aminopyrimidine derivatives, substituted at 5- and 6-positions, were synthesized. The reaction was carried out in a single step by treatment of the corresponding β-ketoester or β-aldehydoester with guanidine hydrochloride in the presence of K2CO3, in a microwave-assisted method without the requirement of solvent. A unique 1:1 co-crystal structure was obtained which shows that a 6-phenyl-2- aminopyrimidinone forms a strong nucleobase-pair with cytosine, involving three hydrogen bonds. The base-pair was found to be as strong as that of natural guanine:cytosine (G:C), signifying the potential application of the synthesized derivatives. Additionally, we also report a second co-crystal involving 5-isopropyl-6-methyl-2-aminopyrimidinone and cytosine in a 1:1 ratio, which also shows strong base-pairing properties. the Partner Organisations 2014.
