s
syringaldehyde
Chemical compound
Also known as Gallaldehyde 3,5-dimethyl ether · 4-hydroxy-3,5-dimethoxybenzaldehyde · 4-hydroxy-3,5-dimethoxy-benzaldehyde
- Formula
- C₉H₁₀O₄
1
- C₉H₁₀O₄
- Mass
- 182.058 Da
1
- 182.058 Da
- Melting point
- 112°C
1
- 112°C
Overview
Chemistry
All data
173 statements · 82% with external sources · numbers in brackets are citations
- Canonical SMILES
- COC1=CC(=CC(=C1O)OC)C=O
1
- COC1=CC(=CC(=C1O)OC)C=O
- Safety classification and labelling
- NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response nfpa health: 1 · nfpa fire: 0 · nfpa instability: 0
- Found in taxon
- Pilocarpus grandiflorus
- Zanthoxylum gilletii
- Populus lasiocarpa
- Populus euphratica
- Posidonia oceanica
- Quercus robur
- Quercus pyrenaica
- Quercus faginea
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- Zizania aquatica
1
- Cinnamomum kotoense
- Cinnamomum subavenium
- Microtropis japonica
3
Sources- 1.Stated in Dihydroagarofuranoid sesquiterpenes, a lignan derivative, a benzenoid, and antitubercular constituents from the stem of Microtropis japonica
- 2.Stated in Antitubercular dihydroagarofuranoid sesquiterpenes from the roots of Microtropis fokienensis
- 3.Stated in New dihydroagarofuranoid sesquiterpenes, a lignan derivative, benzenoid, and antitubercular constituents from the stem of Microtropis japonica
- Mikania laevigata
- Zanthoxylum ailanthoides
6
Sources- 1.Stated in Amides and Benzenoids from Zanthoxylum ailanthoides with Inhibitory Activity on Superoxide Generation and Elastase Release by Neutrophils
- 2.Stated in Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils
- 3.Stated in Chemical Constituents from the Root Bark of FormosanZanthoxylum Ailanthoides
- 4.Stated in Neolignans, a coumarinolignan, lignan derivatives, and a chromene: anti-inflammatory constituents from Zanthoxylum avicennae
- 5.Stated in Constituents of the root wood of Zanthoxylum wutaiense with antitubercular activity
- 6.Stated in New phenylpropenoids, bis(1-phenylethyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integrifoliolum
- Magnolia officinalis
- Isatis tinctoria
- Arabidopsis thaliana
2
Sources- 1.Stated in Metabolomics-oriented isolation and structure elucidation of 37 compounds including two anthocyanins from Arabidopsis thaliana
- 2.Stated in Universally occurring phenylpropanoid and species-specific indolic metabolites in infected and uninfected Arabidopsis thaliana roots and leaves.
- Cissus sicyoides
- Zanthoxylum wutaiense
4
Sources- 1.Stated in Constituents of the root wood of Zanthoxylum wutaiense with antitubercular activity
- 2.Stated in Neolignans, a coumarinolignan, lignan derivatives, and a chromene: anti-inflammatory constituents from Zanthoxylum avicennae
- 3.Stated in Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils
- 4.Stated in New phenylpropenoids, bis(1-phenylethyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integrifoliolum
- Annona montana
- Tetradium glabrifolium
1
- Aralia bipinnata
2
Sources- 1.Stated in Lignans from the wood of Aralia bipinnata
- 2.Stated in Phenylpropanoids from Aralia bipinnata
- Coriandrum sativum
1
- Ilex rotunda
1
- Clausena excavata
- Rhinacanthus nasutus
- Brosimum acutifolium
1
- Gynura elliptica
- Magnolia sinica
- Annona cherimola
- Boronia pinnata
2
Sources- 1.Stated in CONSTITUENTS OF KIGELIA PINNATA
- 2.Stated in Constituents of Boronia pinnata
- Hibiscus cannabinus
- Hydrangea chinensis
- Machilus obovatifolia
- Ficus septica
- Piper solmsianum
- Casearia membranacea
- Hibiscus taiwanensis
- Zanthoxylum nitidum
- Rhizophora apiculata
- Fagraea racemosa
- Gymnosporia pyria
- Phyllostachys nigra
- Mikania shushunensis
- Codonopsis pilosula
- Zanthoxylum integrifoliolum
5
Sources- 1.Stated in New phenylpropenoids, bis(1-phenylethyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integrifoliolum
- 2.Stated in Chemical Constituents from the Root Wood ofZanthoxylum Integrifoliolum
- 3.Stated in Neolignans, a coumarinolignan, lignan derivatives, and a chromene: anti-inflammatory constituents from Zanthoxylum avicennae
- 4.Stated in Constituents of the root wood of Zanthoxylum wutaiense with antitubercular activity
- 5.Stated in Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils
- Daphne feddei
- Panax bipinnatifidus var. bipinnatifidus
- Pisonia aculeata
- Juglans regia
- Senna
- Aframomum giganteum
1
- Gymnadenia conopsea
- Taraxacum formosanum
- Diplospora dubia
- Vepris uguenensis
- Viscum coloratum
- Senra incana
- Vitis vinifera
- Imperata cylindrica
On other databases
29 identifiers linking syringaldehyde across the web's reference databases
- CAS Registry Number134-96-3
- ChEBI ID67380
- ChEMBL IDCHEMBL225303
- ChemSpider ID8333
- DSSTOX compound identifierDTXCID6034182
- DSSTox substance IDDTXSID2059643
- EC number205-167-5
- ECHA Substance Infocard ID100.004.698
- FL number05.153
- Freebase ID/m/02qj4s7
- Human Metabolome Database IDHMDB0258653
- InChIInChI=1S/C9H10O4/c1-12-7-3-6(5-10)4-8(13-2)9(7)11/h3-5,11H,1-2H3
- InChIKeyKCDXJAYRVLXPFO-UHFFFAOYSA-N
- JECFA number1878
- KNApSAcK IDC00007558
- MassBank accession IDMSBNK-RIKEN-PR100983
- Microsoft Academic ID (discontinued)2777411053
- NMRShiftDB structure ID20035535
- NSC number41153
- OpenAlex IDC2777411053
- PDB ligand IDIJV
- Probes And Drugs IDPD065283
- PubChem CID8655
- Reaxys registry number784514
- RTECS numberCU5760000
- SPLASHsplash10-002b-9500000000-648b4cea88c99f600180
- SureChEMBL ID150376
- UniChem compound ID246219
- UNII2ZR01KTT21