I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
4-Pentynoic acid is widely utilized as a building block for the synthesis of eight sequence-defined model oligomers. Due to its triple bond at terminal carbon, it is employed as an intermediate to produce biologically active compounds. It is used as a hypoglycemic agent, which increases liver tyrosine aminotransferase and plasma corticosterone while decreasing blood sugar in rats.
Belger, K.; Krause, N. Smaller, faster, better: modular synthesis of unsymmetrical ammonium salt-tagged NHC-gold(I) complexes and their application as recyclable catalysts in water. Org. Biomol. Chem. 2015, 13 (31), 8556-8560.
Sahariah, P.; Sørensen, K. K.; Hjálmarsdóttir, M. A.; Sigurjónsson, O. E.; Jensen, K. J.; Másson, M.; Thygesen, M. B. Antimicrobial peptide shows enhanced activity and reduced toxicity upon grafting to chitosan polymers. Chem. Commun. 2015, 51 (58), 11611-11614.
Hamano, H.; Nagata, K.; Fukada, N.; Shimotahira, H.; Ju, X.; Ozoe, Y. 5-[4-(3,3-Dimethylbutoxycarbonyl)phenyl]-4-pentynoic acid and its derivatives inhibit ionotropic γ-aminobutyric acid receptors by binding to the 4'-ethynyl-4-n-propylbicycloorthobenzoate site. Bioorg. Med. Chem. 2000, 8 (3), 665-674.
Hazard Statements: H314-H318
Causes severe skin burns and eye damage. Causes serious eye damage.
Precautionary Statements: P260u-P201-P280i-P304+P340-P405-P501a
Obtain special instructions before use. Wear eye/face protection. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.