4-Methoxycinnamaldehyde

• CAS: 1963-36-6
• Catalog Number: ACM1963366
• Category: Inhibitors
• Molecular Weight: 162.19
• Molecular Formula: C10H10O2
• Description: 4-Methoxycinnamaldehyde (p-Methoxycinnamaldehyde), an active constituent of Agastache rugosa, exhibits cytoprotective activity against respiratory syncytial virus (RSV) in human larynx carcinoma cell line. 4-Methoxycinnamaldehyde effectively inhibits cytopathic effect of RSV with an estimated IC50 of 0.055 μg/mL.
• IUPAC Name: (E)-3-(4-methoxyphenyl)prop-2-enal
• Canonical SMILES: COC1=CC=C(C=C1)C=CC=O
• InChI Key: AXCXHFKZHDEKTP-NSCUHMNNSA-N
• Appearance: Powder
• Storage: 4°C, stored under nitrogen*In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen).
• Shipping: Can be shipped at room temperature, where not in use may vary.

Synthetic Use

Upstream Synthesis Route 1

• 624-67-9
• 100-66-3

• 1963-36-6
• 1504-74-1

Reference: [1] Catalysis Science and Technology, 2017, vol. 7, # 19, p. 4422 - 4430

Downstream Synthesis Route 1

• 1963-36-6

• 4964-76-5

Reference: [1] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1984, # 7, p. 1569 - 1572

Downstream Synthesis Route 2

• 1963-36-6
• 17105-65-6

• 43212-67-5

Reference: [1] Synthesis, 2009, # 7, p. 1075 - 1080

Downstream Synthesis Route 3

• 1963-36-6

• 20401-88-1

Reference: [1]Selvam, Parasuraman; Sonavane, Sachin U.; Mohapatra, Susanta K.; Jayaram, Radha V.
[Tetrahedron Letters, 2004, vol. 45, # 15, p. 3071 - 3075]

Downstream Synthesis Route 4

• 1963-36-6

• 4964-76-5

Reference: [1]Journal of the Chemical Society. Perkin transactions I,1984,p. 1569 - 1572

* For details of the synthesis route, please refer to the original source to ensure accuracy.