1258512-07-0

Basic information

• Product Name: (E)-2-(3-(4-methoxyphenyl)-3-oxoprop-1-en-1-yl)benzaldehyde
• Synonyms: (E)-2-(3-(4-methoxyphenyl)-3-oxoprop-1-en-1-yl)benzaldehyde
• CAS NO: 1258512-07-0
• Molecular Weight: 266.296
• Mol File: 1258512-07-0.mol

Chemical Properties

• CAS DataBase Reference: (E)-2-(3-(4-methoxyphenyl)-3-oxoprop-1-en-1-yl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(3-(4-methoxyphenyl)-3-oxoprop-1-en-1-yl)benzaldehyde(1258512-07-0)
• EPA Substance Registry System: (E)-2-(3-(4-methoxyphenyl)-3-oxoprop-1-en-1-yl)benzaldehyde(1258512-07-0)

Safety Data

• Hazardous Substances Data: 1258512-07-0(Hazardous Substances Data)

Upstream product

• 1258512-05-8 (E)-3-(2-(diethoxymethyl)phenyl)-1-(4-methoxyphenyl)prop-2-en-1-one 
• 103890-70-6 2-(diethoxymethyl)benzaldehyde 
• 1777-55-5 (4-methoxyphenacylidene)triphenyl phosphorane 
• 6630-33-7 ortho-bromobenzaldehyde 
• 59259-01-7 2-<2-(1,3-dioxolanyl)>benzaldehyde 
• 1431986-50-3 (E)-3-(2-(1,3-dioxolan-2-yl)phenyl)-1-(4-methoxyphenyl)prop-2-en-1-one 

Downstream Products

• 1258512-39-8 2'-(4-methoxybenzoyl)-1,2'-spirobi[indene]-1,3-dione 
• 118972-71-7 (1H-inden-2-yl)(4-methoxyphenyl)methanone 

Relevant articles and documents

Cobalt-Catalyzed Chemoselective Transfer Hydrogenative Cyclization Cascade of Enone-Tethered Aldehydes

The ligand-free Co-catalyzed chemoselective reductive cyclization cascade of enone-tethered aldehydes with i-PrOH as the environmentally benign hydrogen surrogate is developed by this study. Mechanistic studies disclosed that such a protocol is initiated

Organocatalytic, Enantioselective, intramolecular oxa-michael reaction of alkoxyboronate: A new strategy for enantioenriched 1-substituted 1,3-Dihydroisobenzofurans

An unprecedented strategy for the synthesis of enantioenriched 1-substituted 1,3-dihydroisobenzofurans via an enantioselective oxa-Michael reaction of o-alkoxyboronate containing chalcone (II) has been accomplished employing cinchona alkaloid based squara

Stereoselective synthesis of aminoindanols via an efficient cascade aza-Michael-aldol reaction

An efficient organocatalyzed strategy for the synthesis of 3-amino-1-indanols has been developed. This method is complementary to the conventional Friedel-Crafts strategy. It is also applicable to the synthesis of enantioenriched 3-amino-1-indanols.

NHC-catalyzed spiro bis-indane formation via domino stetter - Aldol - Michael and stetter - Aldol - Aldol reactions

Two novel domino NHC-catalyzed spirocyclizations are described herein, enabling the rapid construction of three new carbon - carbon bonds and a quaternary center with high diastereoselectivity. A variety of spiro bis-indane structures are assembled in a single step from simple o-phthaldialdehyde derivatives.