CAS 6302-94-9

Dihydro-5-methyl-4H-1,3,5-dithiazine

Description:

Dihydro-5-methyl-4H-1,3,5-dithiazine, with the CAS number 6302-94-9, is a heterocyclic compound characterized by a six-membered ring containing two nitrogen atoms and two sulfur atoms. This compound typically exhibits a pale yellow to colorless appearance and is known for its distinctive sulfur and nitrogen functionalities, which contribute to its reactivity and potential applications in organic synthesis. Dihydro-5-methyl-4H-1,3,5-dithiazine is generally soluble in organic solvents, reflecting its non-polar characteristics, while its stability can be influenced by environmental factors such as temperature and light. The presence of the methyl group enhances its chemical properties, making it a subject of interest in various chemical reactions, including those involving nucleophilic substitutions. Additionally, due to its unique structure, it may exhibit biological activity, although specific biological properties would require further investigation. Overall, this compound is of interest in both synthetic chemistry and potential applications in pharmaceuticals or agrochemicals.

Formula: C₄H₉NS₂

InChI: InChI=1S/C4H9NS2/c1-5-2-6-4-7-3-5/h2-4H2,1H3

InChI key: InChIKey=QMWSBGCIPZEDPP-UHFFFAOYSA-N

SMILES: CN1CSCSC1

Synonyms:

• 4H-1,3,5-Dithiazine, dihydro-5-methyl-
• 5-Methyl-1,3,5-Dithiazinane
• Nsc 41551
• Dihydro-5-methyl-4H-1,3,5-dithiazine

Dihydro-5-methyl-4H-1,3,5-dithiazine

Controlled Product

CAS: 6302-94-9

Applications Dihydro-5-methyl-4H-1,3,5-dithiazine is used as a reagent in the synthesis of neovibsanin derivatives which have the ability to induce neuronal differentiation in PC12 cells.
References Annette, P.-J. C., et al.: Tetrahedron, 66, 6842 (2010)

Formula: C₄H₉NS₂

Color and Shape: Neat

Molecular weight: 135.251

Ref: TR-D450320