Methyl-2-isothiocyanatothiophene-3-carboxylate, with the CAS number 126637-07-8, is a chemical compound characterized by its unique structure that includes both isothiocyanate and thiophene functionalities. This compound typically exhibits a yellow to brownish color and is known for its pungent odor, which is characteristic of isothiocyanates. It is soluble in organic solvents, making it useful in various chemical reactions and applications. The presence of the thiophene ring contributes to its aromatic properties, while the isothiocyanate group is known for its reactivity, particularly in nucleophilic substitution reactions. This compound may be utilized in organic synthesis, particularly in the development of agrochemicals or pharmaceuticals, due to its potential biological activity. Additionally, it may exhibit properties such as antimicrobial or herbicidal activity, although specific biological effects would depend on the context of its use and the presence of other functional groups. As with many isothiocyanates, it should be handled with care due to its potential irritant properties.

METHYL-2-ISOTHIOCYANATOTHIOPHENE-3-CARBOXYLATE

126637-07-8: Methyl-2-isothiocyanatothiophene-3-carboxylate, with the CAS number 126637-07-8, is a chemical compound characterized by its unique structure that includes both isothiocyanate and thiophene functionalities. This compound typically exhibits a yellow to brownish color and is known for its pungent odor, which is characteristic of isothiocyanates. It is soluble in organic solvents, making it useful in various chemical reactions and applications. The presence of the thiophene ring contributes to its aromatic properties, while the isothiocyanate group is known for its reactivity, particularly in nucleophilic substitution reactions. This compound may be utilized in organic synthesis, particularly in the development of agrochemicals or pharmaceuticals, due to its potential biological activity. Additionally, it may exhibit properties such as antimicrobial or herbicidal activity, although specific biological effects would depend on the context of its use and the presence of other functional groups. As with many isothiocyanates, it should be handled with care due to its potential irritant properties.

CAS 126637-07-8

METHYL-2-ISOTHIOCYANATOTHIOPHENE-3-CARBOXYLATE

Methyl-2-isothiocyanatothiophene-3-carboxylate

Ref: IN-DA000T0W

Methyl 2-isothiocyanato-3-thiophenecarboxylate

Ref: 54-OR322495

Methyl-2-isothiocyanatothiophene-3-carboxylate

Ref: 10-F019505