CAS 823-09-6

2-(methylsulfanyl)pyrimidine

Description:

2-(Methylsulfanyl)pyrimidine, with the CAS number 823-09-6, is a heterocyclic organic compound characterized by a pyrimidine ring substituted with a methylsulfanyl group at the second position. This compound features a six-membered aromatic ring containing two nitrogen atoms at the 1 and 3 positions, which contributes to its basicity and potential for forming hydrogen bonds. The presence of the methylsulfanyl group enhances its reactivity and solubility in polar solvents. Typically, 2-(methylsulfanyl)pyrimidine exhibits a moderate to high boiling point and melting point, indicative of its molecular interactions. It is often utilized in pharmaceutical and agrochemical research due to its potential biological activity, including antimicrobial and anti-inflammatory properties. Additionally, this compound can serve as a building block in the synthesis of more complex molecules. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly.

Formula: C₅H₆N₂S

InChI: InChI=1/C5H6N2S/c1-8-5-6-3-2-4-7-5/h2-4H,1H3

SMILES: CSc1ncccn1

Synonyms:

• Pyrimidine, 2-(methylthio)-
• 2-(Methylthio)pyrimidine
• 2-(Methylsulfanyl)pyrimidine

Pyrimidine, 2-(methylthio)- (6CI,7CI,8CI,9CI)

CAS: 823-09-6

Formula: C₅H₆N₂S

Purity: 98%

Color and Shape: Liquid

Molecular weight: 126.1795

Ref: IN-DA00G4IO

2-(Methylsulphanyl)pyrimidine

CAS: 823-09-6

2-(Methylsulphanyl)pyrimidine

Formula: C₅H₆N₂S

Purity: 98%

Color and Shape: orange liquid

Molecular weight: 126.18g/mol

Ref: 54-OR15527

2-(Methylthio)pyrimidine

CAS: 823-09-6

Formula: C₅H₆N₂S

Purity: 98%(GC-MS);RG

Color and Shape: Liquid

Molecular weight: 126.18

Ref: 10-F092082

2-Methylthiopyrimidine

CAS: 823-09-6

2-Methylthiopyrimidine is a pyrimido compound that has been shown to inhibit the growth of herpes simplex virus type-1. The synthesis of this molecule is based on an anthranilic acid derivative, which can be reacted with amines to form 2-methylthiopyrimidine and its isomers. This drug has been shown to react with chloride ions and carbon disulphide in metathesis reactions. 2-Methylthiopyrimidine has a pharmacophore that resembles the structure of nucleosides, which are found in many viruses. The chlorine atoms in the 2-methylthiopyrimidine molecule are positioned in such a way that they can bind to the phosphate groups on the surface of the virus, thereby blocking its ability to replicate.

Formula: C₅H₆N₂S

Purity: Min. 95%

Molecular weight: 126.18 g/mol

Ref: 3D-AAA82309