penicillic acid
{{chembox
| Watchedfields = changed
| verifiedrevid = 433999950
| ImageFile = Penicillic acid.svg
| ImageSize = 300px
| ImageAlt = Skeletal formulas of two tautomers
| ImageFile1 = Penicillic-acid-3D-balls.png
| ImageSize1 = 200
| ImageAlt1 = Ball-and-stick model
| IUPACName=5-Hydroxy-5-isopropenyl-4-methoxy-furan-2-one
| OtherNames=
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo=90-65-3
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = ONL14K3AFD
| PubChem=1268111
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = C19495
| SMILES=CC(=C)C1(C=CC(=O)O1)O
}}
|Section2={{Chembox Properties
| C=8 | H=10 | O=4
| Appearance=
| Density=
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|Section3={{Chembox Hazards
| MainHazards=
| FlashPt=
| AutoignitionPt =
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Penicillic acid is a mycotoxin that is produced by Aspergillus flavus and Penicillium roqueforti mold. It is not a product of acid degradation of penicillin. Its first practical synthesis was reported in 1947 by Ralph Raphael, who had worked on penicillin during World War II.{{Cite journal | last1 =Raphael|first1=Ralph | title =Synthesis of the Antibiotic, Penicillic Acid | journal =Nature |volume=160 | year =1947 |issue=4060 | pages = 261–262 |doi=10.1038/160261c0|pmid=20344393 |bibcode=1947Natur.160..261R |s2cid=4066740 }}