CAS 36810-92-1

2-(isothiocyanatomethyl)thiophene

Description:

2-(Isothiocyanatomethyl)thiophene is an organic compound characterized by the presence of both a thiophene ring and an isothiocyanate functional group. The thiophene ring contributes to its aromatic properties, providing stability and potential reactivity in various chemical reactions. The isothiocyanate group, characterized by the functional group -N=C=S, is known for its reactivity, particularly in nucleophilic substitution reactions and as a building block in the synthesis of various bioactive compounds. This compound may exhibit unique physical properties, such as solubility in organic solvents and specific melting or boiling points, influenced by its molecular structure. Additionally, it may possess biological activity, making it of interest in fields such as medicinal chemistry and agrochemicals. The presence of both sulfur and nitrogen in its structure can also lead to interesting interactions in coordination chemistry. Overall, 2-(isothiocyanatomethyl)thiophene is a versatile compound with potential applications in various chemical and pharmaceutical contexts.

Formula: C₆H₅NS₂

InChI: InChI=1/C6H5NS2/c8-5-7-4-6-2-1-3-9-6/h1-3H,4H2

SMILES: c1cc(CN=C=S)sc1

Synonyms:

• 36810-92-1
• Thiophene, 2-(isothiocyanatomethyl)-
• 2-Isothiocyanatomethyl-thiophene

2-(Isothiocyanatomethyl)thiophene

CAS: 36810-92-1

2-(Isothiocyanatomethyl)thiophene is a chemical that belongs to the class of compounds called aliphatic chlorides. It is resistant to hydrochloric acid and aliphatic alcohols. 2-(Isothiocyanatomethyl)thiophene also has active methylene groups, which are reactive with xylene, chlorides, and amines. This chemical may be used in the production of diazo compounds, which are used in the synthesis of polyurethanes.

Formula: C₆H₅NS₂

Purity: Min. 95%

Molecular weight: 155.2 g/mol

Ref: 3D-LBA81092