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2-(Benzyloxy)-5-bromo-N,N-dimethylpyrimidin-4-amine is a pyrimidine derivative with the molecular formula C14H16BrN3O. It features a bromine atom at the 5th position, a benzyloxy group at the 2nd position of the pyrimidine ring, and two N,N-dimethylamine groups attached to the 4th position, classifying it as a tertiary amine. This chemical compound holds potential in the pharmaceutical industry and scientific research due to its unique structural features and reported biological activities.

205672-18-0

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205672-18-0 Usage

Uses

Used in Pharmaceutical Industry:
2-(Benzyloxy)-5-bromo-N,N-dimethylpyrimidin-4-amine serves as a valuable building block for the synthesis of a variety of drug molecules. Its unique structure allows for the creation of new compounds with potential therapeutic applications.
Used in Scientific Research:
As a compound with reported biological activities, 2-(Benzyloxy)-5-bromo-N,N-dimethylpyrimidin-4-amine is an intriguing target for further research and development. It may lead to the discovery of new drugs or contribute to a better understanding of biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 205672-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,6,7 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 205672-18:
(8*2)+(7*0)+(6*5)+(5*6)+(4*7)+(3*2)+(2*1)+(1*8)=120
120 % 10 = 0
So 205672-18-0 is a valid CAS Registry Number.

205672-18-0Downstream Products

205672-18-0Relevant academic research and scientific papers

Studies on the synthesis of the derivatives of 5-(dihydroxyboryl)-cytosines and -isocytosines

Wojtowicz-Rajchel, Hanna,Suchowiak, Marek,Fiedorow, Piotr,Golankiewicz, Krzysztof

, p. 841 - 845 (2007/10/03)

Boron derivatives of isocytosine, containing a dihydroxyboryl group in the 5-position, have been prepared for the first time. Reaction of appropriate pyrimidines with n-butyllithium and subsequent boronation at -100°C with triethylborate, followed by catalytic hydrogenation, gave hydrolytically stable N,N-dimethyl-5-(dihydroxyboryl)isocytosine 8a and N-methyl-5-(dihydroxyboryl)isocytosine 8b. Theoretical calculations suggest that the corresponding boron derivatives of cytosine cannot be obtained as thermodynamically stable compounds.

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