2-Furanone is a heterocyclic organic compound. It is also known as γ-crotonolactone ( GCL ), as it is formally the lactone derived from γ-hydroxy isocrotonic acid . The chemical is colloquially called "butenolide", and is the parent structure for the butenolide class of compounds.

After treatment with chlorine, humic waters contain a range of chloro-furanones, some of which, particularly 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX), are powerful mutagens. The furanones which occur in foods are also mutagenic to bacteria and cause DNA damage in laboratory tests.

Furaneol, or strawberry furanone, is an organic compound used in the flavor and perfume industry. It is formally a derivative of furan . It is a white or colorless solid that is soluble in water and organic solvents.

Jun 1, 2019 · Furanone, a five-membered heteroaromatic ring containing oxygen atom, is of immense pharmaceutical importance. Presence of this nucleus in biologically active compounds of natural and synthetic origin has made it an indispensable motif for design and development of new therapeutic agents.

2(5H)-Furanone | C4H4O2 | CID 10341 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

These furanone analogues are potent anti-infectives and inhibit pathogenic phenotypes in Gram-negative and Gram-positive bacteria as demonstrated in-vitro using gene microarrays, and in-vivo using mouse models.

This result indicated that furanone can be an effective quorum-sensing (QS) inhibiting against many different bacterial genera that produce different types of AHL signal molecules. 98 These compounds suppressed swarming motility by targeting the quorum-sensing receptor.

Jul 29, 2019 · Maple furanone was initially synthesized in 1957 and later identified in hydrolyzed soy protein in 1980, and has been named after its powerful maple-caramel aroma and taste, which is reminiscent...

Sep 11, 2020 · We have covered all reports available on the synthesis of 3(2H)-furanone derivatives and have divided the review into several sections based on the substitution patterns present in the heterocycle. Special emphasis is given to the generality and the mechanistic rationalizations of each methodology.

2(3H)-Furanone | C4H4O2 | CID 140765 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.