82592-68-5

Basic information

• Product Name: 2-Propenoyl chloride, 3-[3,4-bis(acetyloxy)phenyl]-
• CAS NO: 82592-68-5
• Molecular Formula: C13H11ClO5
• Molecular Weight: 282.68
• Mol File: 82592-68-5.mol
• Article Data: 60

Chemical Properties

• CAS DataBase Reference: 2-Propenoyl chloride, 3-[3,4-bis(acetyloxy)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoyl chloride, 3-[3,4-bis(acetyloxy)phenyl]-(82592-68-5)
• EPA Substance Registry System: 2-Propenoyl chloride, 3-[3,4-bis(acetyloxy)phenyl]-(82592-68-5)

Safety Data

• Hazardous Substances Data: 82592-68-5(Hazardous Substances Data)

Upstream product

• 331-39-5 caffeic acid 
• 13788-48-2 di-O-acetylcaffeic acid 
• 331-39-5 caffeic acid 
• 88623-81-8 3,4-diacetoxycinnamic acid 
• 79-37-8 oxalyl dichloride 
• 108-24-7 acetic anhydride 
• 67727-64-4 3,4-diacetoxybenzaldehyde 

Downstream Products

• 141992-29-2 (2S,5R,6R)-6-[2-[(E)-3-(3,4-Diacetoxy-phenyl)-acryloylamino]-2-(4-hydroxy-phenyl)-acetylamino]-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 204273-54-1 (2R,3R)-2,3-Bis-[(E)-3-(3,4-diacetoxy-phenyl)-acryloyloxy]-succinic acid di-tert-butyl ester 
• 1194063-99-4 C₂₃H₂₂N₂O₅ 
• 1073897-83-2 1,4,5-tri-O-caffeoylquinic acid 
• 6082-42-4 3-O-caffeoyl-γ-quinide 

Relevant articles and documents

Sevanol and its analogues: Chemical synthesis, biological effects and molecular docking

Among acid-sensing ion channels (ASICs), ASIC1a and ASIC3 subunits are the most widespread and prevalent in physiological and pathophysiological conditions. They participate in synaptic plasticity, learning and memory, as well as the perception of inflamm

Development trans-N-benzyl hydroxyl cinnamamide based compounds from cinnamic acids and characteristics anticancer potency

The derivatization of three hydroxycinnamamides becomes trans-N-benzylhydroxycinnamamides, and their potential assay as anticancer agents has been carried out. N-benzyl-p-coumaramide (5a), N-benzylcaffeamide (5b), and N-benzylferulamide (5c) were obtained

Novel 3C-like protease inhibitor as well as preparation method and application thereof

The invention provides a novel 3C-like protease inhibitor which is 3 ", 4" - O - diacetyl -epicatechin trans-caffeic acid ester with a specific structure. The invention further provides a preparation method and application of the 3C-like protease inhibitor. The invention has the advantages that the compound 3 ", 4" - O - diacetyl - epicatechin trans-caffeic acid ester is designed and synthesized based on the structure of epicatechin; even when the concentration is low, the activity of 3C-like protease in the novel coronavirus can be obviously inhibited. The compounds can be used as 3C-like protease inhibitors and are used for preparing anti-novel coronavirus SARS-CoV - 2 infection drugs.