3-Chloro-2-cyanothiophene is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a chlorine atom at the 3-position and a cyano group at the 2-position contributes to its unique chemical properties. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular structure allows for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it useful in synthetic organic chemistry. The cyano group imparts notable polarity and reactivity, while the thiophene ring enhances its stability and aromatic character. 3-Chloro-2-cyanothiophene may find applications in the development of pharmaceuticals, agrochemicals, and materials science, particularly in the synthesis of functionalized thiophene derivatives. As with many halogenated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns.

3-Chloro-2-Cyanothiophene

147123-67-9: 2-Thiophenecarbonitrile,3-chloro-(9CI)

3-Chloro-2-cyanothiophene

3-Chloro-2-cyanothiophene is a synthetic compound that can be used in organic synthesis. It has been shown to cleave bonds by nucleophilic activation and is capable of forming five-membered rings with halides, pyrrole, and amines. This compound has also been shown to react thermodynamically with alkyl triazoles. 3-Chloro-2-cyanothiophene is a quaternary ammonium salt that has been shown to activate the nucleophile.

CAS 147123-67-9: 3-Chloro-2-Cyanothiophene

3-Chloro-2-cyanothiophene

Ref: 10-F017089

3-Chloro-2-cyanothiophene

Ref: 3D-XFA12367

3-Chloro-2-Cyanothiophene

Ref: 54-OR1010951

2-Thiophenecarbonitrile, 3-chloro-

Ref: IN-DA001EMV