
1,3-Benzodioxole-5-carboxylic acid
Piperonylic acid is a member of the class of benzodioxoles that is 1,3-benzodioxole substituted by a carboxy group at position 5. It is a natural product isolated from several plant species. It is a selective mechanism-based inactivator of the trans-cinnamate 4-hydroxylase enzyme and exhibits antifungal and skin wound healing properties. It has a role as an EC 1.14.14.91 ( trans-cinnamate 4-monooxygenase) inhibitor, an antifungal agent, a vulnerary and a plant metabolite. It is a monocarboxylic acid, an aromatic carboxylic acid and a member of benzodioxoles. It is a conjugate acid of a piperonylate. — ChEBI
- IUPAC name
- 1,3-benzodioxole-5-carboxylic acid
- Molecular formula
- C8H6O4
- Molecular weight
- 166.13 g/mol
- Exact mass
- 166.02660867 Da
- XLogP3
- 0.4
- Topological polar surface area
- 55.8 Ų
- Hydrogen-bond donors
- 1
- Hydrogen-bond acceptors
- 4
- Covalent units
- 1
- Defined stereocentres
- 0
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:107644
- ChEMBL:CHEMBL573781
- EPA DTXSID:DTXSID6059104
- PubMed:22734410
- PubMed:21489652
- PubMed:19342120
- PubMed:18626717
- PubMed:17229869
- PubMed:16569001
- PubMed:16310363
- PubMed:15913846
- PubMed:15007421
- PubMed:14511910
- PubMed:12376665
- PubMed:11154339
Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.