69998-14-7 Usage
Description
1-(propan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione is a pyrimidine derivative with the molecular formula C8H12N2O3. It features a unique trione functional group, characterized by three carbonyl groups attached to the pyrimidine ring. This chemical compound is widely utilized in organic synthesis and pharmaceutical research as a fundamental building block for constructing more complex molecules. Its structural features and reactivity also make it a promising candidate for the development of new drugs and therapeutic agents. Furthermore, 1-(propan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione may have additional applications in various industrial and research fields, highlighting its versatility and value.
Uses
Used in Organic Synthesis:
1-(propan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione is used as a building block in organic synthesis for constructing more complex molecules. Its unique trione functional group and reactivity facilitate the creation of a variety of chemical compounds with diverse properties and applications.
Used in Pharmaceutical Research:
In pharmaceutical research, 1-(propan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione is employed as a key component in the development of new drugs and therapeutic agents. Its structural features and reactivity make it a valuable candidate for designing innovative pharmaceuticals with potential therapeutic benefits.
Used in Drug Development:
1-(propan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione is utilized in drug development as a starting material or intermediate for synthesizing novel pharmaceuticals. Its unique structural features and reactivity contribute to the creation of new drug candidates with potential therapeutic effects.
Used in Industrial Applications:
1-(propan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione may also have applications in various industrial fields, such as the production of specialty chemicals, materials, or other products. Its versatility and unique properties make it a valuable compound for diverse applications.
Used in Research and Development:
In research and development, 1-(propan-2-yl)pyrimidine-2,4,6(1H,3H,5H)-trione serves as a valuable chemical compound for exploring new reactions, mechanisms, and applications. Its unique structural features and reactivity provide opportunities for advancing scientific knowledge and discovering innovative applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 69998-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,9 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69998-14:
(7*6)+(6*9)+(5*9)+(4*9)+(3*8)+(2*1)+(1*4)=207
207 % 10 = 7
So 69998-14-7 is a valid CAS Registry Number.
69998-14-7Relevant articles and documents
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Stein et al.
, p. 6185,6187 (1956)
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Myosin inhibitor, as well as preparation method and application thereof
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Paragraph 0111; 0115-0116, (2020/02/14)
The invention relates to the field of medicinal chemistry, in particular to a myosin inhibitor, as well as a preparation method and application thereof. The invention provides a compound or pharmacologically acceptable salt, an isomer, a prodrug, a polymorphic substance or a solvate thereof. A chemical structural formula of the compound is as shown in a formula I. Compared with other similar medicines in the prior art, the compound or the pharmacologically acceptable salt, the isomer, the prodrug, the polymorphic substance or the solvate thereof provided by the invention have better activity and a more ideal pharmacokinetics characteristic.
BICYCLIC-PYRIMIDINEDIONE COMPOUNDS
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Paragraph 0144; 0145, (2016/07/27)
The present invention provides novel bicyclic pyrimidinedione compounds that are useful for the treatment of hypertrophic cardiomyopathy (HCM) and conditions associated with left ventricular hypertrophy or diastolic dysfunction. The synthesis and characterization of the compounds is described, as well as methods for treating HCM and other forms of heart disease.