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2,4-dimethoxy-6-(trifluoromethyl)pyrimidine is a pyrimidine derivative with the molecular formula C7H7F3N2O2. It is a white to off-white solid that exhibits a high melting point and is sparingly soluble in water. This chemical compound is valued for its unique structure and properties, making it a crucial building block in the pharmaceutical and agricultural industries.

76513-87-6

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76513-87-6 Usage

Uses

Used in Pharmaceutical Industry:
2,4-dimethoxy-6-(trifluoromethyl)pyrimidine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its incorporation into drug molecules can enhance their therapeutic properties, making it an essential component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-dimethoxy-6-(trifluoromethyl)pyrimidine is utilized as an intermediate in the production of pesticides. Its chemical structure contributes to the effectiveness of these agrochemicals, helping to protect crops from pests and diseases, thereby increasing agricultural productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 76513-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,1 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76513-87:
(7*7)+(6*6)+(5*5)+(4*1)+(3*3)+(2*8)+(1*7)=146
146 % 10 = 6
So 76513-87-6 is a valid CAS Registry Number.

76513-87-6Downstream Products

76513-87-6Relevant academic research and scientific papers

Studies on Organic Fluorine Compounds. Part 35. Trifluoromethylation of Pyrimidine- and Purine-nucleosides with Trifluoromethyl-Copper Complex

Kobayashi, Yoshiro,Yamamoto, Kenjiro,Asai, Toyohira,Nakano, Masanori,Kumadaki, Itsumaro

, p. 2755 - 2761 (2007/10/02)

Halogenated nucleoside derivatives were trifluoromethylated using a solution of a trifluoromethyl-copper complex, which was prepared by shaking trifluoromethyl iodide and copper powder in hexamethylphosphoric triamide and filtering off the excess of copper powder.The following trifluoromethylated nucleosides were obtained in moderate to good yields: 5-trifluoromethyl-uridine, -deoxyuridine, -cytidine, -deoxycytidine, and arabinosylcytosine; 8-trifluoromethyl-adenosine, -deoxyadenosine, and -inosine; and 6-trifluoromethylribofuranosylpurine.This procedure offers simple synthesis of many trifluoromethyl compounds.

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