15101-69-6

Basic information

• Product Name: 3-phenyl-6-methoxy-1H-indene
• Synonyms: 3-phenyl-6-methoxy-1H-indene
• CAS NO: 15101-69-6
• Molecular Weight: 222.287
• Mol File: 15101-69-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-phenyl-6-methoxy-1H-indene(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-6-methoxy-1H-indene(15101-69-6)
• EPA Substance Registry System: 3-phenyl-6-methoxy-1H-indene(15101-69-6)

Safety Data

• Hazardous Substances Data: 15101-69-6(Hazardous Substances Data)

Upstream product

• 479213-87-1 1-(3-methoxyphenyl)-3-phenyl-2-propyn-1ol 
• 5111-70-6 5-methoxy-1-indanone 
• 100-58-3 phenylmagnesium bromide 
• 15101-68-5 1-phenyl-3-(3-(methoxy)phenyl)propan-1-one 
• 7507-86-0 2-bromo-5-methoxy-benzaldehyde 
• 14900-39-1 phenylvinylboronic acid 
• 5470-91-7 3-methoxy-chalcone 

Downstream Products

• 15101-83-4 [2-(5-Methoxy-1-phenyl-indan-1-yl)-ethyl]-dimethyl-amine 
• 131003-31-1 5-methoxy-1-phenyl-1H-inden-2(3H)-one 
• 77605-58-4 2-Benzoyl-5-methoxyphenylacetic acid 
• 1334722-49-4 C₁₆H₁₄O₃ 
• 1334722-09-6 C₁₆H₁₂O₃ 
• 77605-64-2 2-Benzyl-5-methoxyphenylacetic Acid 

Relevant articles and documents

Catalytic Enantioselective [10+4] Cycloadditions

The first peri- and stereoselective [10+4] cycloaddition between catalytically generated amino isobenzofulvenes and electron-deficient dienes is described. The highly stereoselective catalytic [10+4] cycloaddition exhibits a broad scope with high yields,

Synthesis of substituted 4-aroyl-1-indanone and 5-aroyl-1-tetralone

Several substituted 4-aroyl-1-indanones 2 and 5-aroyl-1-tetralones 3 were prepared in good yields from 1-indanones 1 via a series of reasonable transformations.