63644-62-2

Basic information

• Product Name: coniferyl ferulate
• Synonyms: coniferyl ferulate;[(E)-3-(4-Hydroxy-3-methoxyphenyl)prop-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate;3-(4-Hydroxy-3-methoxyphenyl)allyl 3-(4-hydroxy-3-methoxyphenyl)acrylate
• CAS NO: 63644-62-2
• Molecular Formula: C₂₀H₂₀O₆
• Molecular Weight: 356.37
• Mol File: 63644-62-2.mol

Chemical Properties

• Boiling Point: 570.5 °C at 760 mmHg
• Flash Point: 202.8 °C
• Appearance: /
• Density: 1.269 g/cm³
• Vapor Pressure: 1.29E-13mmHg at 25°C
• Refractive Index: 1.64
• Storage Temp.: 2-8°C
• PKA: 8.63±0.20(Predicted)
• CAS DataBase Reference: coniferyl ferulate(CAS DataBase Reference)
• NIST Chemistry Reference: coniferyl ferulate(63644-62-2)
• EPA Substance Registry System: coniferyl ferulate(63644-62-2)

Safety Data

• Hazardous Substances Data: 63644-62-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Applications:
Coniferyl ferulate is used as a potential therapeutic agent for its antioxidant properties, which may contribute to reducing inflammation and potentially mitigating certain types of cancer. coniferyl ferulate's health benefits are currently an active area of research, and its application in pharmaceuticals is being explored for its potential to improve human health.
Used in Agricultural Applications:
In the agricultural industry, coniferyl ferulate is used as a component in the biosynthesis of lignin, which is essential for providing structural support and rigidity to plant cell walls. This contributes to the overall health and stability of plants, making it an important compound in crop production and plant growth.
Used in Food Industry:
Coniferyl ferulate is used as a natural antioxidant in the food industry, particularly in grains such as maize and rice. Its antioxidant properties help to preserve the quality and freshness of these food products, making it a valuable additive in the production of various food items.

InChI:InChI=1/C20H20O6/c1-24-18-12-14(5-8-16(18)21)4-3-11-26-20(23)10-7-15-6-9-17(22)19(13-15)25-2/h3-10,12-13,21-22H,11H2,1-2H3/b4-3+,10-7+

Upstream product

• 65401-83-4 4-acetoxy-3-methoxycinnamaldehyde 
• 20649-42-7 coniferaldehyde 
• 2596-47-6 (E)-3-(4-acetoxy-3-methoxyphenyl)acrylic acid 
• 81766-26-9 4-O-acetyl-coniferyl alcohol 
• 50906-12-2 4-acetoxy-3-methoxycinnamoyl chloride 
• 55882-65-0 4-acetoxyferuloyl chloride 
• 1135-24-6 (E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid 
• 458-35-5 coniferal alcohol 

Downstream Products

• 1135-24-6 (E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid 
• 458-35-5 coniferal alcohol 
• 63644-71-3 (E)-4-(3-methoxy-1-propenyl)-2-methoxyphenol 
• 1135-24-6 3-(4-hydroxy-3-methoxyphenyl)acrylic acid 
• 458-35-5 coniferol 

Relevant articles and documents

p-Coumaroyl-CoA:Monolignol Transferase

The invention relates to nucleic acids encoding a p-coumaroyl-CoA:monolignol transferase and to inhibitory nucleic acids adapted to inhibit the expression and/or translation of a p-coumaroyl-CoA:monolignol transferase RNA. Inhibition of p-coumaroyl-CoA:monolignol transferase in plants improves the incorporation of monolignol ferulates into the lignin of plants, giving rise to plant biomass that is more easily processed into useful products such as paper and biofuels.

Novel c-Met inhibitory olive secoiridoid semisynthetic analogs for the control of invasive breast cancer

Dysregulated receptor tyrosine kinase c-Met and its ligand HGF is valid and attractive molecular target for therapeutic blockade in cancer. Inspired by the chemical structure of the naturally occurring olive secoiridoid (-)-oleocanthal (1) and its documen

Preparation of monolignol γ-acetate, γ-p-hydroxycinnamate, and γ-p-hydroxybenzoate conjugates: Selective deacylation of phenolic acetates with hydrazine acetate

We report here a reliable and facile synthesis of a range of monolignol γ-p-hydroxycinnamate (including p-coumarate, ferulate, and caffeate), γ-acetate, and γ-p-hydroxybenzoate conjugates, many not previously reported, that are either putative intermediat