5-Bromo-6-methyl-4(3H)-pyrimidinone, with the CAS number 3438-52-6, is a heterocyclic organic compound that belongs to the pyrimidine family. This compound features a pyrimidine ring substituted with a bromine atom at the 5-position and a methyl group at the 6-position, along with a keto group at the 4-position, which contributes to its reactivity and potential biological activity. It is typically characterized by its crystalline solid form, and it may exhibit solubility in polar solvents due to the presence of the keto group. The compound is of interest in medicinal chemistry and may serve as a precursor or intermediate in the synthesis of various pharmaceuticals. Its bromine substitution can enhance its reactivity, making it a useful building block in organic synthesis. Additionally, the presence of the methyl group can influence its electronic properties and steric hindrance, affecting its interactions in biological systems. Overall, 5-Bromo-6-methyl-4(3H)-pyrimidinone is a versatile compound with potential applications in drug development and chemical research.

5-Bromo-6-methyl-4(3H)-pyrimidinone

3438-52-6: 4-Pyrimidinol, 5-bromo-6-methyl-, 5-Bromo-6-methyl-4(3H)-pyrimidinone, 4(3H)-Pyrimidinone, 5-bromo-6-methyl-, 4(1H)-Pyrimidinone, 5-bromo-6-methyl-

5-Bromo-6-methylpyrimidin-4-ol is an organic solvent that is used in the preparation of acetone, dimethylsulfoxide and cyclic interferon. It is also present in a number of antiviral agents, such as AZT and 5-bromo-6-(2-(hydroxymethyl)pyrrolidin-1-yl)-5H-[1]pyrrole[3,4,-b]indole. This chemical has been shown to inhibit human leukocytes by binding to proteins on the cell surface. The active form of this chemical is acetaldehyde, which binds to xanthine oxidase and inhibits the formation of uric acid.

CAS 3438-52-6: 5-Bromo-6-methyl-4(3H)-pyrimidinone

5-Bromo-6-methylpyrimidin-4-ol

Ref: 3D-FB154074

5-Bromo-6-methylpyrimidin-4-ol

Ref: 54-OR930487

5-bromo-6-methyl-3,4-dihydropyrimidin-4-one

Ref: 10-F790659

5-Bromo-6-methylpyrimidin-4-ol

Ref: IN-DA003MJD