51940-64-8 Usage
Description
Ethyl 2,4-dichloropyrimidine-5-carboxylate is an organic compound that serves as a crucial intermediate in the synthesis of various chemical products. It is characterized by its chemical structure, which includes a pyrimidine ring with two chlorine atoms at the 2nd and 4th positions and a carboxylate group attached to the 5th position. This structure endows it with versatile reactivity and potential applications in different industries.
Uses
Used in Organic Synthesis:
Ethyl 2,4-dichloropyrimidine-5-carboxylate is used as a key intermediate for the synthesis of various organic compounds. Its unique chemical structure allows for further functionalization and the creation of a wide range of products with diverse applications.
Used in Agrochemical Industry:
In the agrochemical industry, ethyl 2,4-dichloropyrimidine-5-carboxylate is used as a starting material for the development of new pesticides and other agricultural chemicals. Its reactivity and structural features make it a valuable component in the design and synthesis of effective and targeted agrochemicals.
Used in Pharmaceutical Industry:
Ethyl 2,4-dichloropyrimidine-5-carboxylate is employed as an important intermediate in the pharmaceutical industry for the synthesis of various drugs. Its chemical properties enable the development of new therapeutic agents with potential applications in treating a range of medical conditions.
Used in Dyestuff Industry:
In the dyestuff industry, ethyl 2,4-dichloropyrimidine-5-carboxylate is used as a raw material for the production of different types of dyes. Its structural characteristics contribute to the development of novel dyes with improved properties, such as enhanced color strength and stability.
Synthesis Reference(s)
Journal of the American Chemical Society, 64, p. 794, 1942 DOI: 10.1021/ja01256a016
Check Digit Verification of cas no
The CAS Registry Mumber 51940-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,4 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51940-64:
(7*5)+(6*1)+(5*9)+(4*4)+(3*0)+(2*6)+(1*4)=118
118 % 10 = 8
So 51940-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl2N2O2/c1-2-13-6(12)4-3-10-7(9)11-5(4)8/h3H,2H2,1H3
51940-64-8Relevant articles and documents
Atorvastatin that non-preparation method
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Paragraph 0058-0060, (2017/07/01)
The invention relates to a preparation method of avanafil and a new compound provided in a preparation process. According to the method, 5-uracil carboxylic acid or an ester thereof is taken as the raw material, and the avanafil meeting the clinical requirements can be synthesized at a relatively cost; besides, the preparation method is simple and convenient to operate, mild in reaction conditions, high in yield, low in cost, environmentally friendly and suitable for industrial large-scale production of the avanafil.
2,4-Pyrimidinediamine Compounds and Their Uses
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Paragraph 0367, (2015/11/10)
The present invention provides 2,4-pyrimidinediamine compounds that inhibit the IgE and/or IgG receptor signaling cascades that lead to the release of chemical mediators, intermediates and methods of synthesizing the compounds and methods of using the compounds in a variety of contexts, including in the treatment and prevention of diseases characterized by, caused by or associated with the release of chemical mediators via degranulation and other processes effected by activation of the IgE and/or IgG receptor signaling cascades.
THERAPUETIC USES OF SELECTED PYRIMIDINE COMPOUNDS WITH ANTI-MER TYROSINE KINASE ACTIVITY
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Page/Page column 293, (2015/11/03)
Uses of pyrimidines with anti-Mer tyrosine kinase activity as anti-infective agents, immunostimulatory and immunomodulatory agents, anti-cancer agents (including against MerTK -/- tumors and ITD and TKD mutant forms of Acute Myeloid Leukemia (AML)), and as adjunctive agents in combination with chemotherapeutic, radiation or other standard of care for neoplasms.