95280-67-4

Basic information

• Product Name: 3-(benzo[d][1,3]dioxol-5-yl)-1-(4-methoxyphenyl)propan-1-one
• Synonyms: 3-(benzo[d][1,3]dioxol-5-yl)-1-(4-methoxyphenyl)propan-1-one
• CAS NO: 95280-67-4
• Molecular Weight: 284.312
• Mol File: 95280-67-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3-(benzo[d][1,3]dioxol-5-yl)-1-(4-methoxyphenyl)propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(benzo[d][1,3]dioxol-5-yl)-1-(4-methoxyphenyl)propan-1-one(95280-67-4)
• EPA Substance Registry System: 3-(benzo[d][1,3]dioxol-5-yl)-1-(4-methoxyphenyl)propan-1-one(95280-67-4)

Safety Data

• Hazardous Substances Data: 95280-67-4(Hazardous Substances Data)

Upstream product

• 2620-50-0 1,3-benzodioxol-5-ylmethyl amine 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 50479-31-7 1-(3',4'-methylenedioxyphenyl)-3-(4''-methoxyphenyl)propane 
• 15973-65-6 1-(4-methoxyphenyl)cyclopropan-1-ol 
• 94839-07-3 3,4-(methylenedioxy)-benzeneboronic acid 
• 5720-07-0 4-methoxyphenylboronic acid 
• 495-76-1 piperonol 

Downstream Products

• 94675-42-0 2-amino-3-benzo[1,3]dioxol-5-yl-1-(4-methoxy-phenyl)-propan-1-ol 
• 109700-18-7 3-benzo[1,3]dioxol-5-yl-1-(4-methoxy-phenyl)-propane-1,2-dione-2-oxime 

Relevant articles and documents

Pd-catalyzed Oxidative Cross-coupling of Alkyl Chromium(0) Fischer Carbene Complexes with Organoboronic Acids

Alkyl chromium(0) carbene complexes have been explored as the cross-coupling partners in the palladium-catalyzed reaction with aryl or alkenyl boronic acids. This coupling reaction displays the versatile reactivities of alkyl chromium(0) carbenes under palladium catalysis. Mechanistically, this transformation is proposed to involve deprotonation of the alkyl chromium carbene substrate to generate a vinyl chromium anion intermediate that undergoes transmetalation to organopalladium species and reductive elimination.

Structural elucidation, bio-inspired synthesis, and biological activities of cyclic diarylpropanes from Horsfieldia kingii

Bioactivity-guided phytochemical investigation on 70% aqueous acetone extracts of the twigs and leaves of Horsfieldia kingii led to the isolation of two novel cyclic diarylpropanes (1 and 2) bearing a 2,3-dihydro-1H-indene core, one new diarylpropane (3), six known diarylpropanes (4–9), one flavanol (10), and seven lignans (11–17). Their structures were determined by extensive spectroscopic analysis, electronic circular dichroism calculations, and X-ray diffraction crystallography. Moreover, a biomimetic synthesis of 1 and 2 were accomplished in four steps. The in vitro nitric oxide production inhibition tests of these compounds revealed that compounds (±)-2, (+)-2, (?)-2, and 10 were potential with IC50 values lower than 10 μM. Compound 2 could inhibit iNOS expression in LPS-induced RAW264.7 cells at a series of non-cytotoxic concentrations (20 μM). Furthermore, the bioassay results also suggested the primary SARs of 1-phenyl-2,3-dihydro-1H-indene based scaffold.

Synthesis and Structures of Arene Ruthenium (II)–NHC Complexes: Efficient Catalytic α-alkylation of ketones via Hydrogen Auto Transfer Reaction

A panel of six new arene Ru (II)-NHC complexes 2a-f, (NHC?=?1,3-diethyl-(5,6-dimethyl)benzimidazolin-2-ylidene 1a, 1,3-dicyclohexylmethyl-(5,6-dimethyl)benzimidazolin-2-ylidene 1b and 1,3-dibenzyl-(5,6-dimethyl)benzimidazolin-2-ylidene 1c) were synthesized from the transmetallation reaction of Ag-NHC with [(η6-arene)RuCl2]2 and characterized. The ruthenium (II)-NHC complexes 2a-f were developed as effective catalysts for α-alkylation of ketones and synthesis of bioactive quinoline using primary/amino alcohols as coupling partners respectively. The reactions were performed with 0.5?mol% catalyst load in 8?h under aerobic condition and the maximum yield was up to 96%. Besides, the different alkyl wingtips on NHC and arene moieties were studied to differentiate the catalytic robustness of the complexes in the transformations.