1597428-54-0

Basic information

• Product Name: 2-(3,3-dimethylbut-1-ynyl)-4'-methoxybenzophenone
• Synonyms: 2-(3,3-dimethylbut-1-ynyl)-4'-methoxybenzophenone
• CAS NO: 1597428-54-0
• Molecular Weight: 292.378
• Mol File: 1597428-54-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(3,3-dimethylbut-1-ynyl)-4'-methoxybenzophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,3-dimethylbut-1-ynyl)-4'-methoxybenzophenone(1597428-54-0)
• EPA Substance Registry System: 2-(3,3-dimethylbut-1-ynyl)-4'-methoxybenzophenone(1597428-54-0)

Safety Data

• Hazardous Substances Data: 1597428-54-0(Hazardous Substances Data)

Upstream product

• 609-67-6 2-Iodobenzoyl chloride 
• 100-66-3 methoxybenzene 
• 88-67-5 2-Iodobenzoic acid 
• 917-92-0 3,3-Dimethylbut-1-yne 
• 138504-32-2 (2-iodophenyl)(4-methoxyphenyl)methanone 

Downstream Products

• 1597428-57-3 3-(4-methoxyphenyl)-1H-inden-1-one 
• 1597428-59-5 C₂₀H₂₁O₂⁽¹⁺⁾*C₂F₆NO₄S₂^(1-) 

Relevant articles and documents

Stable 1H-Benzo[c]thio- and 1H-Benzo[c]selenophen-2-ium Tetrafluoroborates: Insight into Electronic Structures, Electrochemical Behavior, and Reactivity

The synthesis of 1H-benzo[c]thio- and 1H-benzo[c]selenophen-2-ium tetrafluoroborates by the reaction of triphenylcarbenium tetrafluoroborate with 1-ethylidene-1,3-dihydrobenzo[c]thiophene or 1-ethylidene-1,3-dihydrobenzo[c]selenophene, respectively, is reported. The electronic structure of these novel 1H-benzo[c]chalcogenophenium salts was examined on the basis of their electronic spectra, whereby transitions were assigned in agreement with theoretical calculations. Electrochemical measurements revealed irreversible one-electron reduction waves for these 1H-benzo[c]chalcogenophenium salts.

The First Formation of (1Z)-1-Alkylidene-1H-isobenzofuranium Amides and 1H-Inden-1-ones: Acid-Promoted 5-exo Cyclization and Hydration/Aldol Condensation Reactions of o-Ethynylbenzophenones

(1Z)-1-(2,2-Dimethylpropylidene)-1H-isobenzofuranium bis(trifluoromethylsulfonyl)amides were synthesized through 5-exo cyclization reactions between sterically encumbered o-alkynylbenzophenones and bis(trifluoromethylsulfonyl)imide (Tf2NH). It