101018-40-0

Basic information

• Product Name: 1,1-bis(4-methoxyphenyl)prop-2-en-1-ol
• Synonyms: 1,1-bis(4-methoxyphenyl)prop-2-en-1-ol
• CAS NO: 101018-40-0
• Molecular Weight: 270.328
• Mol File: 101018-40-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,1-bis(4-methoxyphenyl)prop-2-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-bis(4-methoxyphenyl)prop-2-en-1-ol(101018-40-0)
• EPA Substance Registry System: 1,1-bis(4-methoxyphenyl)prop-2-en-1-ol(101018-40-0)

Safety Data

• Hazardous Substances Data: 101018-40-0(Hazardous Substances Data)

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 90-96-0 bis(p-methoxyphenyl)methanone 
• 3536-96-7 vinylmagnesium chloride 
• 728-87-0 4,4'-Dimethoxybenzhydrol 
• 123-11-5 4-methoxy-benzaldehyde 
• 1826-67-1 vinyl magnesium bromide 
• 1312210-79-9 C₁₈H₂₀O₃ 

Downstream Products

• 19618-37-2 3,3-Bis-(4'-methoxyphenyl)propenal 
• 1616781-57-7 3-(diphenylphosphoryl)-1,2-bis(4-methoxyphenyl)propan-1-one 
• 21757-10-8 1,2-Di-(p-methoxyphenyl)-4-phenyl-butan-1,4-dion 
• 79754-50-0 ethyl 2-ethoxycarbonyl-4,5-bis-p-methoxyphenyl-5-oxopentanoate 
• 28656-26-0 3,3-Bis(4-methoxyphenyl)[3H]naphtho[2,1-b]pyran 
• 79754-47-5 4,5-bis(4-methoxyphenyl)-5-oxopentanenitrile 
• 54043-37-7 4,4,4-trifluoro-1,2-bis(4-methoxyphenyl)butan-1-one 
• 1116366-55-2 2,2-di(4-methoxyphenyl)-3-(1-naphthylmethyl)oxirane 

Relevant articles and documents

Synthesis and Photochromism of Novel Pyridyl-Substituted Naphthopyrans

Multitarget synthetic strategies to access novel photochromic 3H-naphtho[2,1-b]pyrans decorated with pyridyl units are described. The new pyridyl-substituted 3H-naphtho[2,1-b]pyrans display good photochromic properties with reversible generation of photomerocyanines, which exhibit mainly orange/red hues. Photochromic parameters including photocolorability and persistence of color vary tremendously on structural modification of the naphthopyran core.

Electrochemical Oxidative Aryl(alkyl)trifluoromethylation of Allyl Alcohols via 1,2-Migration

An electrochemical oxidative difunctionalization of allyl alcohols for the synthesis of β-trifluoromethyl ketones is achieved through a 1,2-migration process. A series of β-trifluoromethyl ketones can be facilely obtained utilizing CF3SO2

Visible light-mediated arylalkylation of allylic alcohols through concomitant 1,2-aryl migration

A photocatalytic process for selective arylalkylation of allylic alcohols with α-bromo diethyl malonate has been developed. The reaction provided a straightforward approach to synthesize α-aryl-β-alkylated ketones via unique 1,2-aryl migration. The procedure is highlighted by its operational simplicity and mild reaction conditions.