CAS 1073-54-7

4-(Methylthio)-2-pyrimidinamine

Description:

4-(Methylthio)-2-pyrimidinamine, with the CAS number 1073-54-7, is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at the 1 and 3 positions. This compound features a methylthio group (-S-CH3) at the 4-position and an amino group (-NH2) at the 2-position of the pyrimidine ring, contributing to its reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit solubility in polar solvents due to the presence of the amino group. The compound is of interest in medicinal chemistry and may be studied for its potential applications in pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Its properties, such as melting point, boiling point, and spectral characteristics, can vary based on purity and environmental conditions. Safety data should be consulted for handling and storage, as with any chemical substance.

Formula: C₅H₇N₃S

InChI: InChI=1S/C5H7N3S/c1-9-4-2-3-7-5(6)8-4/h2-3H,1H3,(H2,6,7,8)

InChI key: InChIKey=DTGVQKUDTNRETI-UHFFFAOYSA-N

SMILES: S(C)C1=NC(N)=NC=C1

Synonyms:

• 2-Amino-4-(methylthio)pyrimidine
• 2-Pyrimidinamine, 4-(methylthio)-
• 4-(Methylsulfanyl)Pyrimidin-2-Amine
• 4-(Methylthio)-2-pyrimidinamine
• 4-Methylthio-2-aminopyrimidine
• NSC 43261
• Pyrimidine, 2-amino-4-(methylthio)-

4-(Methylsulfanyl)pyrimidin-2-amine

CAS: 1073-54-7

4-(Methylsulfanyl)pyrimidin-2-amine is a benzoyl derivative of pyrimidin-2-amine. It is a heterocyclic compound that can be synthesized from the reaction of cyanamide and benzoyl chloride. 4-(Methylsulfanyl)pyrimidin-2-amine is used as an intermediate in organic synthesis to produce other compounds.

Formula: C₅H₇N₃S

Purity: Min. 95%

Molecular weight: 141.2 g/mol

Ref: 3D-BAA07354