For research use only. Not for therapeutic Use.
5-Chloro-2-thiophenecarbonyl chloride (Cat No.: R030296) is a reactive heterocyclic acyl chloride derived from thiophene, featuring a chlorine atom at the 5-position and a carbonyl chloride group at the 2-position. It is commonly used as a building block in organic synthesis, particularly for preparing thiophene-based derivatives, pharmaceuticals, and agrochemicals. The acyl chloride functionality enables facile coupling with amines, alcohols, or thiols to form amides, esters, or thioesters. Its electron-rich thiophene ring contributes to bioactivity and functional versatility in medicinal chemistry applications.
CAS Number | 42518-98-9 |
Synonyms | 5-Chloro-2-thenoyl Chloride; 5-Chloro-2-thienoyl Chloride; 5-Chloro-2-thienylcarbonyl Chloride; 5-Chloro-2-thiophenecarbonyl Chloride;?5-Chlorothiophen-2-carboxylic Acid Chloride? |
Molecular Formula | C5H2Cl2OS |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | 5-chlorothiophene-2-carbonyl chloride |
InChI | InChI=1S/C5H2Cl2OS/c6-4-2-1-3(9-4)5(7)8/h1-2H |
InChIKey | BMPDCQVRKDNUAP-UHFFFAOYSA-N |
SMILES | C1=C(SC(=C1)Cl)C(=O)Cl |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |