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
• Article Data: 3

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

General Description

Coniferyl ferulate is a complex chemical compound which is primarily found in plants. It is a class of phenolic compound known for its antioxidant properties and is commonly seen in a variety of grains including maize and rice. Coniferyl ferulate is critically involved in the biosynthesis of lignin, a polymeric substance that adds rigidity to plant cell walls. Additionally, recent research has suggested that this compound may potentially exhibit health benefits such as reducing inflammation and mitigating certain kinds of cancer. However, these potential benefits are still an active area of research and more studies are required to fully understand the health effects of coniferyl ferulate.

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

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

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.

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