23674-15-9

Basic information

• Product Name: Anthracene, 9-(4-methoxyphenyl)-
• CAS NO: 23674-15-9
• Molecular Formula: C21H16O
• Molecular Weight: 284.357
• Mol File: 23674-15-9.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: Anthracene, 9-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Anthracene, 9-(4-methoxyphenyl)-(23674-15-9)
• EPA Substance Registry System: Anthracene, 9-(4-methoxyphenyl)-(23674-15-9)

Safety Data

• Hazardous Substances Data: 23674-15-9(Hazardous Substances Data)

Upstream product

• 120-12-7 anthracene 
• 4346-59-2 para-methoxyphenyldiazonium chloride 
• 716-53-0 9-chloroanthracene 
• 35692-27-4 triethoxy(4-methoxyphenyl)silane 
• 696-62-8 para-iodoanisole 
• 100622-34-2 anthracene-9-boronic acid 
• 121-98-2 methyl 4-methoxybenzoate 
• 61592-89-0 2,2’-dibromodiphenylmethane 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 90-44-8 anthracen-9(10H)-one 
• 5720-07-0 4-methoxyphenylboronic acid 
• 1401613-67-9 C₃₁H₃₆O₅ 
• 288570-39-8 (2-benzoylphenyl)(4-methoxyphenyl)methanone 
• 3586-83-2 1-(4-methoxy-phenyl)-3-phenyl-isobenzofuran 

Downstream Products

• 24672-76-2 9,10-bis-(4-methoxy-phenyl)-anthracene 
• 59012-47-4 10-Methoxy-10-p-methoxyphenyl anthron 
• 210096-12-1 9-(4-hydroxyphenyl)-anthracene 
• 1469711-69-0 10-(4-methoxyphenyl)anthracene-9-carbaldehyde 
• 124562-67-0 [10b-(4-Methoxy-phenyl)-2-phenyl-6b,10b-dihydro-1-oxa-benzo[2,3]pentaleno[1,6-ab]inden-10c-yl]-phenyl-methanone 

Relevant articles and documents

Sterically enhanced 2-iminopyridylpalladium chlorides as recyclable ppm-palladium catalyst for Suzuki–Miyaura coupling in aqueous solution

Sterically hindered 2-iminopyridine derivatives and their palladium chlorides complexes are designed and prepared, which efficiently promote the Suzuki–Miyaura coupling (SMC) reaction in aqueous solution. Besides the good to excellent yields and broad substrate scope, these catalysts can be reused for at least four new batches of the substrates. Spontaneous separation of coupling products in the aqueous reaction medium is the additional striking feature of this catalytic process. Furthermore, catalytic performance of palladium complexes bearing the azo-bridged phenyl groups was greatly influenced by the UV irradiation due to the cis/trans photoisomerization of azo unit of the catalysts. In conclusion, titled palladium complexes provide a green, sustainable, cost-effective, and convenient process to synthesize SMC products at multi-gram-scale reaction.

Double-anthracene D-delta-A type dark blue organic fluorescent material, and preparation method and application thereof

The invention relates to a double-anthracene D-delta-A type dark blue organic fluorescent material, and a preparation method and an application thereof. The structural formula of the material is shownin the specification; and in the formula, R1 is an elec

D-A type organic blue fluorescent material as well as preparation method and application thereof

The invention relates to a D-A type organic blue fluorescent material as well as a preparation method and application thereof. The molecular design strategy of the material is to take benzene as a central pi-conjugated bridge chain, and connect two anthra