63449-52-5

Basic information

• Product Name: 4,4'-DIACETOXYSTILBENE
• Synonyms: 4,4'-DIACETOXYSTILBENE;stilbene-4,4'-diyl diacetate;4 4-DIACETOXYSTILBENE 95%;Diacetic acid (ethene-1,2-diyl)bis-p-phenylene ester;Diacetic acid [4,4'-(1,2-ethenediyl)bisbenzene]-1,1'-diyl ester
• CAS NO: 63449-52-5
• Molecular Formula: C₁₈H₁₆O₄
• Molecular Weight: 296.32
• EINECS: 264-153-7
• Product Categories: Stilbenes (substituted)
• Mol File: 63449-52-5.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4,4'-DIACETOXYSTILBENE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-DIACETOXYSTILBENE(63449-52-5)
• EPA Substance Registry System: 4,4'-DIACETOXYSTILBENE(63449-52-5)

Safety Data

• Hazardous Substances Data: 63449-52-5(Hazardous Substances Data)

Usage

Uses

Used in Biochemical and Pharmacological Research:
4,4'-DIACETOXYSTILBENE is used as a fluorescent probe for visualizing and tracking cellular processes and molecular interactions. Its fluorescent properties allow researchers to monitor biological events in real-time, providing valuable insights into various physiological and pathological mechanisms.
Used in Drug Development:
Due to its anti-inflammatory, antioxidant, and cancer-preventive properties, 4,4'-DIACETOXYSTILBENE is considered a potential candidate for the development of new drugs. These drugs could potentially treat a range of conditions, from inflammatory diseases to cancer, by leveraging the compound's inherent therapeutic properties.
Used in Cancer Research:
4,4'-DIACETOXYSTILBENE has been studied for its potential role in inhibiting the growth of certain types of cancer cells. This application focuses on understanding the compound's mechanism of action and its ability to target specific cancer cells, with the goal of developing targeted cancer therapies.
Used in the Medical Field:
In the medical field, 4,4'-DIACETOXYSTILBENE's potential applications extend beyond research and drug development. Its properties may contribute to the advancement of diagnostic tools, therapeutic strategies, and preventive measures for various diseases, particularly those related to inflammation and cancer.
Used in Biotechnology:
The biotechnology industry can benefit from 4,4'-DIACETOXYSTILBENE's fluorescent properties and potential therapeutic effects. It may be incorporated into biosensors, imaging techniques, and other biotechnological applications that require the tracking and analysis of biological processes at the molecular level.

Upstream product

• 2628-16-2 p-acetoxystyrene 
• 393827-07-1 (S)-2-vinyl-piperidine-1-carboxylic acid tert-butyl ester 
• 70122-89-3 tert-butyl allyl carbonate 
• 2971-36-0 2,2-bis(p-hydroxyphenyl)-1,1,1-trichloroethane 
• 127-09-3 sodium acetate 
• 108-24-7 acetic anhydride 
• 855409-29-9 4,4'-diacetoxy-α,α'-dichloro-bibenzyl 
• 659-22-3 4,4'-dihydroxystilbene 

Downstream Products

• 99-96-7 4-hydroxy-benzoic acid 

Relevant articles and documents

Stereoselective total synthesis of alkaloid caulophyllumine B using iterative olefin cross-metathesis protocol

Herein we report the first total synthesis of alkaloid caulophyllumine B in 14 steps by an iterative olefin cross-metathesis strategy from l-glutamic acid.

Preparation of Boc-protected cinnamyl-type alcohols: A comparison of the Suzuki-Miyaura coupling, cross-metathesis, and Horner-Wadsworth-Emmons approaches and their merit in parallel synthesis

Three synthetic strategies for the construction of tert-butyl (E)-3-arylprop-2-en-1-ol carbonates are described. Complementary approaches employing Suzuki-Miyaura coupling and cross-metathesis reaction gave moderate yields of the title compounds in one-step, both methods are suitable for high-throughput and parallel chemistry. A detailed investigation into the Suzuki-Miyaura coupling reaction is provided along with the studies on the synthesis of pinacolyl 1-(tert-butyloxycarbonyl)propenol-3-ylboronate, the key building block. Conventional synthesis of the title compounds via the Horner-Wadsworth-Emmons reaction as a key step in a three-step-one-purification protocol was optimized and the results are compared with those of the latter reactions.