872857-74-4

Basic information

• Product Name: 2-(2,4-dimethoxyphenyl)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one
• Synonyms: 2-(2,4-dimethoxyphenyl)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one
• CAS NO: 872857-74-4
• Molecular Weight: 312.365
• Mol File: 872857-74-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(2,4-dimethoxyphenyl)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4-dimethoxyphenyl)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(872857-74-4)
• EPA Substance Registry System: 2-(2,4-dimethoxyphenyl)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(872857-74-4)

Safety Data

• Hazardous Substances Data: 872857-74-4(Hazardous Substances Data)

Upstream product

• 872857-72-2 acetic acid 2-bromo-6-methoxy-3,4-dihydro-naphthalen-1-yl ester 
• 133730-34-4 2,4-dimethoxyphenylboronic acid 
• 17715-69-4 1-Bromo-2,4-dimethoxybenzene 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 

Relevant articles and documents

5-Carba-pterocarpens: A new scaffold with anti-HCV activity

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Synthesis of 5-carbapterocarpens by α-arylation of tetralones followed by one-pot demethylation/cyclization with BBr3

5-Carbapterocarpens, one of them displaying estrogenic activity, were prepared from α-aryltetralones in high yields through a one-pot, BBr 3-promoted O-demethylation and cyclization sequence. The key α-aryltetralone intermediates were obtained

Tetracyclic compounds as estrogen ligands

This invention provides estrogen receptor modulators having the structure: wherein R1, R2, R3, R4, Q, n, R8, R9, R10, and R11 have been defined in the specification; o