53781-03-6

Basic information

• Product Name: 9(10H)-Anthracenone, 10-[(4-methoxyphenyl)methylene]-
• CAS NO: 53781-03-6
• Molecular Formula: C22H16O2
• Molecular Weight: 312.368
• Mol File: 53781-03-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 9(10H)-Anthracenone, 10-[(4-methoxyphenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: 9(10H)-Anthracenone, 10-[(4-methoxyphenyl)methylene]-(53781-03-6)
• EPA Substance Registry System: 9(10H)-Anthracenone, 10-[(4-methoxyphenyl)methylene]-(53781-03-6)

Safety Data

• Hazardous Substances Data: 53781-03-6(Hazardous Substances Data)

Upstream product

• 529-86-2 9-anthrol 
• 123-11-5 4-methoxy-benzaldehyde 
• 90-44-8 anthracen-9(10H)-one 

Downstream Products

• 17407-24-8 9-(4-methoxybenzyl)anthracene 
• 579504-79-3 10-(4-methoxybenzyl)-9(10H)-anthracenone 

Relevant articles and documents

Novel benzylidene-9(10H)-anthracenones as highly active antimicrotubule agents. Synthesis, antiproliferative activity, and inhibition of tubulin polymerization

A novel series of 10-benzylidene-9(10H)-anthracenones and 10-(phenylmethyl)-9(10H)-anthracenones were synthesized and evaluated for antiproliferative activity in an assay based on K562 leukemia cells. The 3-hydroxy-4-methoxybenzylidene analogue 9h was fou

Characterization of a new class of androgen receptor antagonists with potential therapeutic application in advanced prostate cancer

The human androgen receptor plays a major role in the development and progression of prostate cancer and represents a well-established drug target. All clinically approved androgen receptor antagonists possess similar chemical structures and exhibit the s

Synthesis and antitumor activity of 10-substituted benzylidene anthrone

Fifteen compounds of 10-substituted benzylidene anthrone were prepared with moderate yield by reaction of anthrone and substituted benzaldehydes under the presence of pyridine and piperidine as catalyst. Their antitumor activities in vitro were evaluated.