105705-48-4

Basic information

• Product Name: 3-(4-methoxyphenyl)chroman-4-one
• CAS NO: 105705-48-4
• Molecular Weight: 254.285
• Mol File: 105705-48-4.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 3-(4-methoxyphenyl)chroman-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxyphenyl)chroman-4-one(105705-48-4)
• EPA Substance Registry System: 3-(4-methoxyphenyl)chroman-4-one(105705-48-4)

Safety Data

• Hazardous Substances Data: 105705-48-4(Hazardous Substances Data)

Upstream product

• 100-66-3 methoxybenzene 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 491-37-2 2,3-dihydro-4H-1-benzopyran-4-one 
• 139449-21-1 3-phenylthio-2,3-dihydro-(4H)-benzopyran-4-one 
• 1776-09-6 3-bromochroman-4-one 
• 153488-86-9 3-(allyloxycarbonyl)chroman-4-one 
• 18649-43-9 4-methoxyphenyllead(IV) triacetate 
• 824-94-2 p-methoxybenzyl chloride 
• 79744-47-1 1-(2-hydroxyphenyl)-2-(4-methoxyphenyl)ethanone 
• 611-20-1 salicylonitrile 
• 90-02-8 salicylaldehyde 
• 768-60-5 4-methoxyphenylacetylen 
• 1621-58-5 3-(4-methoxyphenyl)-4H-chromen-4-one 
• 153488-91-6 allyl 3-(4-methoxyphenyl)-4-oxochroman-3-carboxylate 

Downstream Products

• 1621-58-5 3-(4-methoxyphenyl)-4H-chromen-4-one 
• 145917-96-0 3-(4-methoxyphenyl)-2H-chromene 

Relevant articles and documents

Enantioselective construction of sterically hindered tertiary α-aryl ketones: A catalytic asymmetric synthesis of isoflavanones

A method for the catalytic asymmetric α-arylation of ketones bearing very sterically hindered aryl rings has been developed. This reaction occurs under mild conditions, in short reaction times and has been applied to the first catalytic asymmetric synthesis of isoflavanones.

Palladium-catalyzed direct arylation of 4-chromanones: Selective synthesis of racemic isoflavanones and 3,3-diaryl-4-chromanones

For the first time, the synthesis of racemic isoflavanones has been achieved in satisfactory to good yields and with high selectivity by Pd-catalyzed direct C-3 arylation of 3-unsubstituted 4-chromanones with aryl bromides with the aid of a Pd2(dba)3/tBu 3PHBF4 catalyst system in the presence of KHCO3 as the base in a dioxane/water mixture (4:1). This catalyst system has also been employed in an unprecedented synthesis of 3,3-diaryl-4-chromanones through direct arylation of 4-chromanones in water.

Rapid syntheses of (±)-pterocarpans and isoflavones via the gold-catalyzed annulation of aldehydes and alkynes

(±)-Pterocarpan and analogues (4a-c) have been synthesized efficiently via the annulation of salicylaldehydes (1a, 1b and 1c) and o-methoxymethoxylphenylacetylene (2a), followed by a one-pot reduction and acidic cyclization of the ketones (3a-c). In addition, isoflavone derivatives (5a-c) have been synthesized rapidly, in two steps, via the annulation of salicylaldehyde (1a) and arylacetylenes (2b, 2c and 2d), followed by IBX/DMSO oxidation of the isoflavanones (3d, 3e and 3f).