CAS 1194-22-5

6-Hydroxy-2-methyl-4(1H)-pyrimidinone

Description:

6-Hydroxy-2-methyl-4(1H)-pyrimidinone, with the CAS number 1194-22-5, is a heterocyclic organic compound characterized by a pyrimidine ring structure that features a hydroxyl group and a methyl group. This compound is known for its role in various biochemical processes, particularly in the context of nucleic acid metabolism and as a potential precursor in the synthesis of nucleotides. The presence of the hydroxyl group contributes to its reactivity and solubility in polar solvents, while the methyl group influences its steric properties. 6-Hydroxy-2-methyl-4(1H)-pyrimidinone can exhibit tautomerism, which may affect its chemical behavior and interactions with other molecules. It is also of interest in medicinal chemistry due to its potential biological activities, including antimicrobial and antiviral properties. As with many pyrimidine derivatives, it may participate in hydrogen bonding, which can influence its stability and reactivity in various chemical environments.

Formula: C₅H₆N₂O₂

InChI: InChI=1S/C5H6N2O2/c1-3-6-4(8)2-5(9)7-3/h2H,1H3,(H2,6,7,8,9)

InChI key: InChIKey=BPSGVKFIQZZFNH-UHFFFAOYSA-N

SMILES: O=C1C=C(O)N=C(C)N1

Synonyms:

• 2-Methyl-4,6-Dihydroxy Pyrimidine
• 2-Methyl-4,6-dihydroxypyrimidine
• 2-Methyl-4,6-hydroxypyrimidine
• 2-Methyl-4,6-pyrimidinediol
• 2-Methyl-Pyrimidine-4,6-Diol
• 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl-
• 4,6-Dihydroxy-2-methylpyrimidine
• 4,6-Dihydroxyl-2-Methylpyrimidine
• 4,6-Pyrimidinediol, 2-methyl-
• 4,6-Pyrimidinediol,2-methyl- (6CI,7CI)
• 6-Hydroxy-2-methyl-4(1H)-pyrimidinone
• 6-Hydroxy-2-methylpyrimidin-4(3H)-one

4,6-Dihydroxy-2-methylpyrimidine

CAS: 1194-22-5

Formula: C₅H₆N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 126.1133

Ref: IN-DA000IOT

6-hydroxy-2-methyl-3,4-dihydropyrimidin-4-one

CAS: 1194-22-5

6-hydroxy-2-methyl-3,4-dihydropyrimidin-4-one

Purity: 97%

Molecular weight: 126.11g/mol

Ref: 54-OR22311

4,6-Dihydroxy-2-methylpyrimidine

CAS: 1194-22-5

4,6-Dihydroxy-2-methylpyrimidine is an organic compound that is synthesized by the reaction of 2-chloroethanol with ethyl chloroformate and nitroethane in the presence of a magnesium salt. The synthesis can be done systematically or by chance. 4,6-Dihydroxy-2-methylpyrimidine can be formed by the hydrolysis of ethyl esters with a metallacycle. Its acidic properties are due to its electron withdrawing groups. The systematic synthesis is carried out in two steps: 1) formation of the monomers from ethyl chloroformate and nitroethane; 2) condensation of the monomers to form 4,6-dihydroxy-2-methylpyrimidine. This synthesis requires hydroxide solution and chloroformate as well as a base such as sodium hydroxide or potassium hydroxide. The chemical reaction mechanism is based

Formula: C₅H₆N₂O₂

Purity: Min. 95%

Molecular weight: 126.11 g/mol

Ref: 3D-FD30738

2-Methyl-4,6-dihydroxypyrimidine

CAS: 1194-22-5

Formula: C₅H₆N₂O₂

Purity: 97.0%

Color and Shape: Brown powder

Molecular weight: 126.115

Ref: 10-F036424