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2-Amino-3-methylpyrimidin-4(3H)-one is an organic compound with the molecular formula C5H6N2O. It is a heterocyclic molecule, specifically a pyrimidine derivative, which is characterized by the presence of two nitrogen atoms in the ring structure. 2-aMino-3-MethylpyriMidin-4(3H)-one is a white crystalline solid and is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those containing pyrimidine rings. It is also known as 3-methyluracil or 3-methyl-2,4-dihydroxypyrimidin-5-one. The compound is used as a building block in the preparation of nucleosides, nucleotides, and other biologically active molecules, making it a valuable chemical in the fields of medicinal chemistry and chemical biology.

2417-17-6

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2417-17-6 Usage

General Description

2-amino-3-methylpyrimidin-4(3H)-one is a chemical compound with the molecular formula C5H6N2O. It is a heterocyclic organic compound that contains both an amino group and a carbonyl group. 2-aMino-3-MethylpyriMidin-4(3H)-one is important in the biological synthesis of various molecules, including the coenzyme NADH. It also has potential applications in pharmaceutical research and development, particularly in the design and synthesis of new drugs. Additionally, it is used as a precursor in the synthesis of various pyrimidine derivatives and other biologically active compounds. Overall, 2-amino-3-methylpyrimidin-4(3H)-one is a versatile chemical with a variety of potential applications in the fields of medicine and chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 2417-17-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2417-17:
(6*2)+(5*4)+(4*1)+(3*7)+(2*1)+(1*7)=66
66 % 10 = 6
So 2417-17-6 is a valid CAS Registry Number.

2417-17-6Downstream Products

2417-17-6Relevant academic research and scientific papers

Structural Alteration of Nucleic Acid Bases by Bromomalonaldehyde

Nair, Vasu,Offerman, Rick J.,Turner, Gregory A.

, p. 4021 - 4025 (1984)

Bromomalonaldehyde (BMDA), prepared by bromination of malonaldehyde with elemental bromine, has been employed to modify a number of nucleic acid bases.These reactions transform pyrimidine and purine bases into modified systems containing etheno and etheno carboxaldehyde moieties, among other products.The structures of these modified bases were established by UV, mass spectral, and high-field NMR data.Fluorescence emission data for some of the adducts are of significance.The general mechanism of modification is discussed.

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