106511-71-1

Basic information

• Product Name: 1-Propanone, 2-bromo-1-(4-methoxyphenyl)-3-phenyl-
• CAS NO: 106511-71-1
• Molecular Formula: C16H15BrO2
• Molecular Weight: 319.198
• Mol File: 106511-71-1.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 2-bromo-1-(4-methoxyphenyl)-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 2-bromo-1-(4-methoxyphenyl)-3-phenyl-(106511-71-1)
• EPA Substance Registry System: 1-Propanone, 2-bromo-1-(4-methoxyphenyl)-3-phenyl-(106511-71-1)

Safety Data

• Hazardous Substances Data: 106511-71-1(Hazardous Substances Data)

Upstream product

• 113450-88-7 (E)-1-(2,3,4,5,6-pentamethylphenyl)-3-phenylprop-2-en-1-one 
• 100-66-3 methoxybenzene 
• 100-39-0 benzyl bromide 
• 100-07-2 4-methoxy-benzoyl chloride 
• 645-45-4 hydrocinnamic acid chloride 
• 501-52-0 3-Phenylpropionic acid 
• 100-52-7 benzaldehyde 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 22966-19-4 trans-4'-methoxychalcone 
• 5739-38-8 1-(4-methoxyphenyl)-3-phenylpropan-1-one 

Downstream Products

• 1245904-69-1 N-[5-benzyl-4-(4-hydroxyphenyl)-1,3-selenazol-2-yl]-3,4-dihydroxybenzamide 
• 1245904-68-0 N-[5-benzyl-4-(4-methoxyphenyl)-1,3-selenazol-2-yl]-3,4-dimethoxybenzamide 
• 1446017-81-7 5-benzyl-4-(4-methoxyphenyl)-N-(naphthalen-2-ylmethyl)thiazol-2-amine 
• 1446017-82-8 5-benzyl-4-(4-methoxyphenyl)-N-(pyridin-3-ylmethyl)thiazol-2-amine 
• 1446017-78-2 5-benzyl-N-(furan-2-ylmethyl)-4-(4-methoxyphenyl)thiazol-2-amine 
• 1446017-84-0 5-benzyl-4-(4-methoxyphenyl)-N-(3,4,5-trimethoxybenzyl)thiazol-2-amine 
• 1446017-75-9 4-((5-benzyl-4-(4-methoxyphenyl)thiazol-2-ylamino)methyl)-2-methoxyphenol 
• 1621006-44-7 2-((5-benzyl-4-(4-methoxyphenyl)thiazol-2-ylamino)methyl)-4-nitrophenol 
• 1446017-83-9 5-benzyl-N-(2,6-dichlorobenzyl)-4-(4-methoxyphenyl)thiazol-2-amine 
• 1446017-89-5 5-benzyl-4-(4-methoxyphenyl)-N,N-dimethylthiazol-2-amine 
• 1446017-93-1 4-(5-benzyl-2-(diethylamino)thiazol-4-yl)phenol 
• 1446017-90-8 5-benzyl-N,N-diethyl-4-(4-methoxyphenyl)thiazol-2-amine 
• 1003313-16-3 5-benzyl-2-chloro-4-(4-methoxyphenyl)thiazole 

Relevant articles and documents

Pentamethylphenyl (Ph*) and Related Derivatives as Useful Acyl Protecting Groups for Organic Synthesis: A Preliminary Study

A study of acyl protecting groups derived from the Ph? motif is reported. While initial studies indicated that a variety of functional groups were not compatible with the Br 2-mediated cleavage conditions required to release the Ph? group, strategies involving the use of different reagents or a modification of Ph? itself (Ph*OH) were investigated to solve this problem.

2, 4, 5-trisubstituted selenazole class compound and its preparation method, composition and use thereof

The invention relates to 2,4,5-trisubstituted selenazole compounds and a preparation method, a composition and application thereof, in particular to compounds in a formula (I), or all possible isomers, predrugs, pharmaceutically acceptable salts, solvates or hydrates thereof, wherein each substituent is shown as the description. The invention also relates to a method for preparing the compounds in the formula (I), medicinal compositions comprising the compounds in the formula (I), and application of the compounds in the formula (I) or the medicinal compositions in preparation of medicines for treating and/or preventing phospholipid transfer protein (PLTP) activity increase and/or diseases or syndromes related with the phospholipid transfer protein activity increase. The compounds in the formula (I) have good effect of inhibiting the PLTP activity and/or cholesteryl ester transfer protein (CETP) activity of blood plasma, and can be used for treating diseases on the basis.

Kinetic diastereomer differentiation in Au(III)- and Bi(III)-catalyzed benzylic arylation: Concise and stereocontrolled synthesis of 2-amino-1,1-diarylalkanes

Benzylic alcohols carrying an adjacent α-nitro or α-azido group on the alkane chain are converted into syn-1,1-diaryl-2-nitro- and 2-azidoalkanes with electron-rich arenes in stereoselective reactions catalyzed by Bronsted and Lewis acids. Gold(III) chloride and bismuth(III) triflate were found to be especially efficient as catalysts, showing kinetically controlled differentiation in the reactivity of diastereomeric α-substituted benzyl alcohols. Applications to therapeutically relevant syn- and anti- 2-amino-1,1-diarylalkanes are projected.