1111237-76-3 Usage
Description
5-Bromo-4-chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine is a heterocyclic chemical compound with the molecular formula C7H5BrClN3. It features a pyrimidine ring with bromo, chloro, and methyl substituents, making it a valuable building block in organic synthesis and medicinal chemistry for the development of pharmaceutical drugs. Its unique structure and properties have been studied for potential biological activities, showing promise in the treatment of various diseases.
Uses
Used in Pharmaceutical Drug Development:
5-Bromo-4-chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine is used as a key intermediate in the synthesis of complex molecules for drug discovery and development. Its unique structure allows for the creation of new pharmaceutical compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 5-Bromo-4-chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block for the creation of various organic compounds. Its reactivity and functional groups enable the formation of diverse chemical entities with potential applications in different industries.
Used in Medicinal Chemistry Research:
5-Bromo-4-chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine is utilized in medicinal chemistry research to explore its potential biological activities and evaluate its efficacy in treating various diseases. Its unique structure and properties make it a promising candidate for further investigation and development as a therapeutic agent.
Used in Drug Discovery:
As a heterocyclic compound with specific functional groups, 5-Bromo-4-chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine is employed in drug discovery to identify new lead compounds with potential therapeutic benefits. Its unique chemical properties and reactivity contribute to the development of innovative pharmaceutical drugs.
Used in Chemical Research:
5-Bromo-4-chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine is also used in chemical research to study its properties, reactivity, and potential applications in various chemical processes. Understanding its behavior in different chemical reactions can lead to the development of new synthetic routes and methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 1111237-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,1,2,3 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1111237-76:
(9*1)+(8*1)+(7*1)+(6*1)+(5*2)+(4*3)+(3*7)+(2*7)+(1*6)=93
93 % 10 = 3
So 1111237-76-3 is a valid CAS Registry Number.
