684220-30-2 Usage
Uses
Used in Research Applications:
4,6-dichloro-2-Pyrimidinecarboxylic acid is used as a research chemical for the synthesis of more complex compounds and in the study of chemical reactions and properties. Its unique structure allows for the exploration of its reactivity and potential applications in various fields.
Used in Pharmaceutical Industry:
4,6-dichloro-2-Pyrimidinecarboxylic acid is used as an intermediate in the synthesis of pharmaceutical compounds. Its presence in the molecular structure can contribute to the development of new drugs with specific therapeutic properties, making it a valuable component in the creation of novel medications.
Used in Chemical Synthesis:
4,6-dichloro-2-Pyrimidinecarboxylic acid is used as a building block in the synthesis of a wide range of chemical products. Its reactivity and structural features make it a key component in the production of various substances, from dyes to agrochemicals, and more.
Used in Material Science:
4,6-dichloro-2-Pyrimidinecarboxylic acid is used in the development of new materials with specific properties. Its incorporation into the molecular structure of these materials can lead to the creation of materials with unique characteristics, such as improved stability, reactivity, or other desirable traits.
Check Digit Verification of cas no
The CAS Registry Mumber 684220-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,4,2,2 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 684220-30:
(8*6)+(7*8)+(6*4)+(5*2)+(4*2)+(3*0)+(2*3)+(1*0)=152
152 % 10 = 2
So 684220-30-2 is a valid CAS Registry Number.
684220-30-2Relevant academic research and scientific papers
Pyrimidine derivatives as IL-8 receptor antagonists
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Page 12, (2010/02/06)
Compounds containing the pyrimidine nucleus and their use to treat diseases and conditions related to inappropriate Interleukin-8 receptor activity are disclosed. The compounds are of the formula I In these compounds, Q is preferably unsubstituted and substituted heterocyclyl; U is usually hydrogen or fluorine; and V is preferably hydrogen, halogen, alkyl, —O—alkyl or —S-alkyl. A representative example is: