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(E)-2-(2,6-dimethoxy-5-nitropyrimidin-4-yl)-N,N-dimethylethenamine is a complex organic chemical compound with the molecular formula C12H16N4O5. It features a pyrimidine core, which is substituted with a nitro group at the 5-position and two methoxy groups at the 2 and 6 positions. The molecule also contains a double-bonded ethylamine side chain with two methyl groups attached to the nitrogen atoms, giving it a (E)-configuration. (E)-2-(2,6-dimethoxy-5-nitropyrimidin-4-yl)-N,N-dimethylethenamine is known for its potential applications in medicinal chemistry, particularly as a precursor in the synthesis of various biologically active molecules. Its structure and properties make it a subject of interest for researchers exploring new drug candidates and chemical entities with specific therapeutic effects.

83256-18-2

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83256-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83256-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,2,5 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83256-18:
(7*8)+(6*3)+(5*2)+(4*5)+(3*6)+(2*1)+(1*8)=132
132 % 10 = 2
So 83256-18-2 is a valid CAS Registry Number.

83256-18-2Relevant academic research and scientific papers

Synthetic Strategies toward the Synthesis of 2,4-Dimethoxypyrrolopyrimidine

Cupps, Thomas L.,Wise, Dean S.,Townsend, Leroy B.

, p. 1060 - 1064 (2007/10/02)

Two approaches to prepare 2,4-dimethoxypyrrolopyrimidine (1) are described. 2,4-Dimethoxy-6-methyl-5-nitropyrimidine (2) was converted to 6-(cyanomethyl)-2,4-dimethoxy-5-nitropyrimidine (6) in two steps.Subsequent catalytic hydrogenation of 6 produced 1.In a second approach, 2 was formylated, giving rise to 6--2,4-dimethoxy-5-nitropyrimidine (7).Hydrogenation of 7 resulted in the formation of 1.Reduction of 2 provided 5-amino-2,4-dimethoxy-6-methylpyrimidine (10).Reaction of compound 10 with triethyl orthoformate produced 2,4-dimethoxy-5--6-methylpyrimidine (11).Reaction of 11 with lithium diisopropylamide gave 2,4-dimethoxy-5-isocyano-6-methylpyrimidine (12).

REACTION OF DIMETHYLFORMAMIDE DIMETHYLACETAL WITH METHYLPYRIMIDINES

Prikazchikova, L. P.,Khutova, B. M.,Cherkasov, V. M.

, p. 746 - 748 (2007/10/02)

The reaction of dimethylformamide dimethylacetal with methylpyrimidines and methyltriazines was studied, and β-dimethylaminovinylpyrimidines and β-dimethylaminovinyltriazines were obtained.It is shown that electron-acceptor substituents facilitate the rea

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