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3,4-(Methylenedioxy)cinnamic acid, 99%, predominantly trans|303371|2373-80-0

3,4-(Methylenedioxy)cinnamic acid, 99%, predominantly trans

Cat. No JK303371_100_G
J&K Chemical

Product Information

Product Name
3,4-(Methylenedioxy)cinnamic acid, 99%, predominantly trans
Brand Name
J&K
Product Number
303371
CAS
2373-80-0
Molecular Formula
C10H8O4
Molecular Weight
192.17
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
3-(1,3-Benzodioxol-5-yl)propenoic acid
PubChem CID
643181
IUPAC Name
(E)-3-(1,3-benzodioxol-5-yl)prop-2-enoic acid
InChI Key
QFQYZMGOKIROEC-DUXPYHPUSA-N
SMILES
C1OC2=C(O1)C=C(C=C2)/C=C/C(=O)O

Properties

Melting Point
242-244

Safety Information

GHS Symbols
Hazard Symbol
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Synthesis, Properties, and Application Fields of Hindered Monoterpenes and Their Derivatives
Publication Name: Doklady Chemistry
Publication Date: 2025-04
DOI: 10.1134/s001250082560052x

Immunocompromisation of wheat host by L-BSO and 2,4-DPA induces susceptibility to the fungal pathogen Fusarium oxysporum
Publication Name: Stress Biology
Publication Date: 2024-04-09
DOI: 10.1007/s44154-023-00137-7

Enhancing Chemical Diversity of Fungal Secondary Metabolite by OSMAC Strategy
Publication Name: Fungi Bioactive Metabolites
Publication Date: 2024
DOI: 10.1007/978-981-99-5696-8_18

Piperonal synthase from black pepper (Piper nigrum) synthesizes a phenolic aroma compound, piperonal, as a CoA-independent catalysis
Publication Name: Applied Biological Chemistry
Publication Date: 2022-03-24
DOI: 10.1186/s13765-022-00691-0

Synthesis from Diarylamines
Publication Name: Science of Synthesis
Publication Date: 2022

3,4-(Methylenedioxy)cinnamic acid, 99%, predominantly trans

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