70402-10-7

Usage

Uses

Used in Pharmaceutical Industry:
6-Hydroxy-4H-furo[3,2-c]pyran-2(6H)-one is used as an antibiotic and antibacterial agent for its ability to inhibit the growth of certain bacteria and fungi.
Used in Food Industry:
6-Hydroxy-4H-furo[3,2-c]pyran-2(6H)-one is used as a contaminant control agent to prevent the growth of harmful microorganisms in food products.
Used in Agriculture:
6-Hydroxy-4H-furo[3,2-c]pyran-2(6H)-one is used as a plant toxin to protect crops from harmful pests and diseases.

InChI:InChI=1/C7H6O4/c8-6-2-5-4(3-10-6)1-7(9)11-5/h1-2,6,8H,3H2

Upstream product

• 158044-97-4 O-methyl neopatulin 
• 18449-76-8 methyl α-D-lyxopyranoside 
• 135234-98-9 C₇H₆O₄ 
• 131149-12-7 methyl 4--4-deoxy-2,3-O-isopropylidene-β-L-erythro-pentopyranoside 
• 131149-15-0 (6S,7S,7aS)-7-hydroxy-6-methoxy-7,7a-dihydrofuro<3,2-c>pyran-2(4H,6H)-one 
• 60562-98-3 methyl 2,3-O-isopropylidene-α-D-lyxopyranoside 
• 87-72-9 D-lyxose 
• 22596-25-4 methyl 2,3-O-isopropylidene-β-L-erythro-pentopyranosid-4-ulose 
• 158044-94-1 2-<(tert-butyl)dimethylsiloxy>-4-<<(tert-butyl)dimethylsiloxy>methyl>furan 
• 131149-16-1 (S)-O-methylneopatulin 

Relevant academic research and scientific papers

An Efficient Total Synthesis of Neopatulin

A new, highly efficient synthesis of neopatulin (1) has been achieved through Lewis acid-catalysed aldol reaction of 2-formyl-1,3-dithiane (4) with 2-(tert-butyldimethylsiloxy)-4-furan (5).

Divergent synthesis of the co-isolated mycotoxins longianone, isopatulin, and (Z)-ascladiol via furan oxidation

(Chemical Equation Presented) Longianone and the biosynthetically related mycotoxins isopatulin and (Z)-ascladiol were prepared following a divergent route from a readily available furan diol. The route toward longianone features an unprecedented TBAF-pro

Ylidenebutenolide Mycotoxins. Concise Syntheses of Patulin and Neopatulin from Carbohydrate Precursors

Conversion of arabinose 10 to the protected ketone 13 followed by Wittig condensation to 14, acidcatalysed cyclisation (to lactone 16), dehydration and deprotection provides a brief synthesis of the mycotoxic substance patulin 1, which is produced by Penicillium and Aspergillus spp.In a similar manner, the biogenetic precursor to patulin, neopatulin 8, is synthesized from lyxose 25 via the key intermediates 24, 28 and 30.