2-Thiophenecarbonitrile, 5-iodo- is an organic compound characterized by the presence of a thiophene ring, a five-membered aromatic heterocycle containing sulfur, and a cyano group (-C≡N) attached to the carbon adjacent to the sulfur atom. The compound also features an iodine atom substituted at the 5-position of the thiophene ring, which can influence its reactivity and physical properties. Typically, compounds like this exhibit moderate solubility in organic solvents and may have distinct spectral characteristics in NMR and IR spectroscopy due to the presence of the cyano and iodo functional groups. The presence of the cyano group suggests potential applications in organic synthesis and materials science, while the iodine substituent may facilitate further chemical transformations, such as nucleophilic substitutions. Overall, 2-Thiophenecarbonitrile, 5-iodo- is of interest in various fields, including pharmaceuticals and agrochemicals, due to its unique structural features and potential reactivity.

2-Thiophenecarbonitrile,5-iodo-

18945-81-8: 2-Cyano-5-iodothiophene, 5-Iodo-2-thiophenecarbonitrile

2-Thiophenecarbonitrile, 5-iodo-

5-Iodothiophene-2-carbonitrile

5-Iodo-2-thiophenecarbonitrile, also known as 5-iodo-2-benzothiophene, is a benzothiophene that has been dehydrated to form a five-membered singlet. This compound is used as a transient and has yielded high yields of furan in a photocleavage reaction. 5-Iodo-2-thiophenecarbonitrile can be synthesized from methylcyclohexane with the use of Wittig reactions. It is also a good sensitizer for photochemical reactions due to its nucleophilic nature.

CAS 18945-81-8: 2-Thiophenecarbonitrile,5-iodo-

2-Thiophenecarbonitrile, 5-iodo-

Ref: IN-DA002DP0

5-Iodothiophene-2-carbonitrile

Ref: 10-F232824

5-Iodo-2-thiophenecarbonitrile

Ref: 3D-FI148933