223432-94-8 Usage
Description
Pyrrolo[1,2-c]pyrimidine-1,4-dione, 2,3-dihydro(9CI), also known as 2,3-dihydropyrrolo[1,2-c]pyrimidine-1,4-dione, is a heterocyclic chemical compound with the molecular formula C6H5N3O2. It features a pyrrolopyrimidine ring system with a pyrimidine-1,4-dione core, which endows it with unique structural and potential pharmacological properties.
Uses
Used in Medicinal Chemistry and Drug Development:
Pyrrolo[1,2-c]pyrimidine-1,4-dione, 2,3-dihydro(9CI) is utilized as a promising candidate in medicinal chemistry and drug development due to its distinctive structure and potential pharmacological activities. Its unique ring system may contribute to the development of new therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, Pyrrolo[1,2-c]pyrimidine-1,4-dione, 2,3-dihydro(9CI) serves as a valuable building block for the preparation of other chemical compounds. Its versatile structure allows for the creation of a variety of derivatives with different properties and applications.
Used as a Building Block for Chemical Compounds:
Pyrrolo[1,2-c]pyrimidine-1,4-dione, 2,3-dihydro(9CI) is also used as a building block in the synthesis of other complex organic molecules. Its presence in these compounds can influence their reactivity, stability, and potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 223432-94-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,4,3 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 223432-94:
(8*2)+(7*2)+(6*3)+(5*4)+(4*3)+(3*2)+(2*9)+(1*4)=108
108 % 10 = 8
So 223432-94-8 is a valid CAS Registry Number.
223432-94-8Relevant articles and documents
Synthesis of 1,2-dihydropyrrolo[1,2-c]pyrimidin-l-ones
Alvarez, Mercedes,Fernandez, David,Joule, John A.
, p. 249 - 255 (2007/10/03)
1,2-Dihydropyrrolo[1,2-c]pyrimidin-1-ones 2 have been synthesised from pyrrole. We have developed a versatile procedure for the introduction of substituents into the pyrrolopyrimidinones 2, at positions 5 or 7 as desired, and as required by our plans for
