CAS 127667-02-1: 3-Thiophenecarbonitrile, 2-chloro-

Description: 3-Thiophenecarbonitrile, 2-chloro- is an organic compound characterized by the presence of a thiophene ring, a carbonitrile functional group, and a chlorine substituent. The thiophene ring contributes to the compound's aromatic properties, which can influence its reactivity and stability. The carbonitrile group (-C≡N) is known for its strong electron-withdrawing nature, which can enhance the compound's reactivity in nucleophilic addition reactions. The chlorine atom, located at the second position of the thiophene ring, can also affect the electronic distribution and steric hindrance, potentially influencing the compound's behavior in chemical reactions. This compound may be of interest in various fields, including pharmaceuticals and materials science, due to its unique structural features that can lead to diverse applications. Additionally, its properties such as solubility, boiling point, and melting point would depend on the specific interactions between its functional groups and the surrounding environment. Overall, 3-Thiophenecarbonitrile, 2-chloro- presents a combination of characteristics that make it a subject of interest in organic chemistry.

Formula: C₅H₂ClNS

InChI: InChI=1S/C5H2ClNS/c6-5-4(3-7)1-2-8-5/h1-2H

InChI key: InChIKey=QHEASGMGAALVJB-UHFFFAOYSA-N

SMILES: N#CC=1C=CSC1Cl

Synonyms:

• 2-Chlorothiophene-3-carbonitrile
• 3-Thiophenecarbonitrile, 2-chloro-

3-Thiophenecarbonitrile, 2-chloro-

CAS: 127667-02-1

• Formula: C₅H₂ClNS
• Molecular weight: 143.5941

2-Chlorothiophene-3-carbonitrile

CAS: 127667-02-1

• Purity: 95+%
• Molecular weight: 143.58999633789062

2-Chlorothiophene-3-carbonitrile

CAS: 127667-02-1

Versatile small molecule scaffold

• Formula: C₅H₂ClNS
• Purity: Min. 95%
• Molecular weight: 143.59 g/mol