548796-81-2

Basic information

• Product Name: 1,1-di(p-methoxyphenyl)-3-phenylpropargyl alcohol
• Synonyms: 1,1-di(p-methoxyphenyl)-3-phenylpropargyl alcohol
• CAS NO: 548796-81-2
• Molecular Weight: 344.41
• Mol File: 548796-81-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,1-di(p-methoxyphenyl)-3-phenylpropargyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-di(p-methoxyphenyl)-3-phenylpropargyl alcohol(548796-81-2)
• EPA Substance Registry System: 1,1-di(p-methoxyphenyl)-3-phenylpropargyl alcohol(548796-81-2)

Safety Data

• Hazardous Substances Data: 548796-81-2(Hazardous Substances Data)

Upstream product

• 90-96-0 bis(p-methoxyphenyl)methanone 
• 4440-01-1 lithium phenylacetylide 
• 536-74-3 phenylacetylene 

Downstream Products

• 17665-76-8 3,3-bis(4-methoxyphenyl)-1-phenylprop-2-en-1-one 
• 118769-17-8 2,8-dimethoxy-5,11-bis-(4-methoxy-phenyl)-6,12-diphenyl-naphthacene 
• 1092071-67-4 C₅₂H₄₀O₂ 
• 1266570-28-8 diethyl 3,3-bis(4-methoxyphenyl)-1-phenylpropa-1,2-dienyl(4-methoxyphenyl)phosphoramidate 
• 1266570-27-7 diethyl 3,3-bis(4-methoxyphenyl)-1-phenylpropa-1,2-dienyl(p-tolyl)phosphoramidate 
• 1264635-88-2 N-(2-iodo-6-methoxy-3-(4-methoxyphenyl)-1-phenyl-1H-inden-1-yl)-4-methylbenzenesulfonamide 
• 1415035-13-0 4-iodo-5,5-bis(4-methoxyphenyl)-3-phenyl-2-tosyl-2,5-dihydroisoxazole 
• 1616101-39-3 1,2-bis(4-methoxyphenyl)-4-phenyl-9H-carbazole 
• 1616101-43-9 6-methoxy-1,2-bis(4-methoxyphenyl)-4-phenyl-9H-carbazole 
• 1616101-47-3 1,2-bis(4-methoxyphenyl)-9-methyl-4-phenyl-9H-carbazole 
• 1616101-48-4 1,2-bis(4-methoxyphenyl)-4-phenyl-9-(prop-2-ynyl)-9H-carbazole 
• 1616101-52-0 N-((3-(3,3-bis(4-methoxyphenyl)-1-phenylprop-1,2-dienyl)-1-methyl-1H-indol-2-yl)methyl)-4-methylbenzenesulfonamide 
• 1616101-68-8 C₃₃H₂₆⁽²⁾HNO₂ 

Relevant articles and documents

2,2,4,6-Tetraaryl-2H-benzo[h]chromenes: The influence of electronic communication between aryl substituents on their photochromism

A series of photochromic 2,2,4,6-tetraaryl-2H-benzo[h]chromenes have been efficiently synthesised by two complementary strategies employing the condensation of 1,1,3-triarylprop-2-yn-1-ols with 4-substituted 1-naphthols and Suzuki cross-coupling chemistry

The influence of a 1,1-diarylvinyl moiety on the photochromism of naphthopyrans

1,1,3-Triarylpent-4-en-1-yn-3-ols, efficiently obtained in two steps from 1,1,3-triarylprop-2-yn-1-ols by a Meyer-Schuster rearrangement and subsequent addition of lithium trimethylsilylacetylide, react with either a 1- or 2- naphthol to afford photochrom