CAS 392238-35-6
:5-bromo-N-prop-2-en-1-ylthiophene-2-carboxamide
Description:
5-Bromo-N-prop-2-en-1-ylthiophene-2-carboxamide is a chemical compound characterized by its unique structure, which includes a thiophene ring, a bromine substituent, and an amide functional group. The presence of the bromine atom enhances its reactivity and can influence its electronic properties, making it potentially useful in various chemical applications, including organic synthesis and materials science. The prop-2-en-1-yl group introduces an alkene functionality, which can participate in further chemical reactions such as polymerization or cross-coupling reactions. This compound may exhibit interesting biological activities due to the thiophene moiety, which is often found in pharmaceuticals and agrochemicals. Additionally, the carboxamide group can engage in hydrogen bonding, affecting solubility and interaction with biological targets. Overall, 5-bromo-N-prop-2-en-1-ylthiophene-2-carboxamide presents a versatile scaffold for further chemical exploration and potential applications in various fields, including medicinal chemistry and materials development.
Formula:C8H8BrNOS
InChI:InChI=1/C8H8BrNOS/c1-2-5-10-8(11)6-3-4-7(9)12-6/h2-4H,1,5H2,(H,10,11)
SMILES:C=CCNC(=O)c1ccc(Br)s1
Synonyms:- 2-thiophenecarboxamide, 5-bromo-N-2-propen-1-yl-
- N-Allyl-5-bromothiophene-2-carboxamide
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