88623-81-8

Basic information

• Product Name: (E)-Caffeic Acid Diacetate
• Synonyms: (E)-Caffeic Acid Diacetate;3-[3,4-Bis(acetyloxy)phenyl]-2-propenoic Acid
• CAS NO: 88623-81-8
• Molecular Formula: C₁₃H₁₂O₆
• Molecular Weight: 264.23078
• Product Categories: Aromatics
• Mol File: 88623-81-8.mol
• Article Data: 84

Chemical Properties

• Appearance: /
• Solubility: Chloroform, Dichloromethane
• CAS DataBase Reference: (E)-Caffeic Acid Diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-Caffeic Acid Diacetate(88623-81-8)
• EPA Substance Registry System: (E)-Caffeic Acid Diacetate(88623-81-8)

Safety Data

• Hazardous Substances Data: 88623-81-8(Hazardous Substances Data)

Usage

Uses

Protected Caffeic Acid (C080000), a constituent of plants.

Upstream product

• 331-39-5 caffeic acid 
• 108-24-7 acetic anhydride 
• 127-09-3 sodium acetate 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 331-39-5 cis-caffeic acid 
• 331-39-5 caffeic acid 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 67727-64-4 3,4-diacetoxybenzaldehyde 
• 141-82-2 malonic acid 

Downstream Products

• 98631-72-2 3,4-diacetoxycinnamoyl chloride 
• 331-39-5 caffeic acid 
• 57142-64-0 3,4-diacetoxystyrene 
• 1224851-63-1 2-acetoxy-benzoic acid 2-[3-(3,4-di-acetoxy-phenyl)-acryloyloxy]-ethyl ester 
• 82592-68-5 (E)-3,4-di-O-acetylcaffeoyl chloride 
• 849589-35-1 C₁₇H₁₅NO₈ 
• 64-19-7 acetic acid 
• 66417-50-3 (E)-methyl 3-(3,4-diacetoxyphenyl)acrylate 
• 769970-69-6 (2S,4R) methyl 1-[(E)-3-(3,4-diacetyloxyphenyl)-2-propenoyl]-4-[(4-methylphenyl)sulfonyl]oxy-2-pyrrolidinecarboxylate 
• 769970-67-4 (2S,4R) methyl 1-[(E)-3-(3,4-diacetyloxyphenyl)-2-propenoyl]-4-[(methylsulfonyl)oxy]-2-pyrrolidinecarboxylate 
• 769970-65-2 (2S,4R) methyl 1-[(E)-3-(3,4-diacetyloxyphenyl)-2-propenoyl]-4-hydroxy-2-pyrrolidinecarboxylate 

Relevant articles and documents

Total Synthesis and Structural Elucidation of (-)-Cephalezomine G

The first asymmetric synthesis and configurational elucidation of (-)-cephalezomine G was achieved. The highly functionalized Cα-substituted proline derivative was prepared from d-proline as the only chiral source via a C → N → C chirality transfer method

Design, synthesis of Cinnamyl-paeonol derivatives with 1, 3-Dioxypropyl as link arm and screening of tyrosinase inhibition activity in vitro

This study aimed to obtain tyrosinase inhibitors for treating hyperpigmentation. A series of cinnamyl ester analogues were designed and synthesized with cinnamic acid (CA) and peaonol compounds. The safety, melanin content and inhibitory effects of all ta

Oat polyphenol avenanthramide-2c confers protection from oxidative stress by regulating the Nrf2-ARE signaling pathway in PC12 cells

Accumulating evidence has demonstrated that cellular antioxidant systems play essential roles in retarding oxidative stress-related diseases, such as Parkinson's disease. Because nuclear factor erythroid 2-related factor 2 (Nrf2) is a chief regulator of c

Preparation method and application of hydroxyl cinnamyl ester type catechin

The invention relates to a preparation method and application of hydroxyl cinnamyl ester type catechins. The hydroxyl cinnamyl ester type catechins comprise four catechins which are respectively namedas epicatechin trans-coumarate, epicatechin trans-caffeic acid ester, epigallocatechin trans-coumarate and epigallocatechin trans-caffeic acid ester. The hydroxyl cinnamyl ester type catechins are prepared by the following steps: carrying out four steps of full acetylation on epicatechin and epigallocatechin, removal of acetyl on phenolic hydroxyl, silanizing of phenolic hydroxyl and removal of 3-acetyl, then respectively esterifying with acetylated caffeic acid or coumaric acid acyl chloride, and removing a protecting group. The preparation method of the four catechins is simple and mild inconditions, and can be completed under general experimental conditions. The four hydroxycinnamyl ester type catechins have a certain inhibition effect on the activity of alpha-glucosidase, can be usedfor hypoglycemic drugs, and have important significance in the fields of agriculture and medicine.