60333-75-7

Basic information

• Product Name: 1-BroMo-2-(2-propen-1-yloxy)-benzene
• Synonyms: 1-BroMo-2-(2-propen-1-yloxy)-benzene
• CAS NO: 60333-75-7
• Molecular Formula: C₉H₉BrO
• Molecular Weight: 213.07116
• Product Categories: Aromatics, Intermediates
• Mol File: 60333-75-7.mol
• Article Data: 30

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 1-BroMo-2-(2-propen-1-yloxy)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BroMo-2-(2-propen-1-yloxy)-benzene(60333-75-7)
• EPA Substance Registry System: 1-BroMo-2-(2-propen-1-yloxy)-benzene(60333-75-7)

Safety Data

• Hazardous Substances Data: 60333-75-7(Hazardous Substances Data)

Usage

Uses

1-Bromo-2-(2-propen-1-yloxy)-benzene is used as a reagent to produce high yield (97%) 3-methyl-2,3-dihydrobenzofurans through reductive radical cyclization reactions.

Upstream product

• 95-56-7 2-hydroxybromobenzene 
• 5441-16-7 1-(allyloxy)-2,4-dichlorobenzene 
• 179938-94-4 (Z)-1-bromo-2-(prop-1-en-1-yloxy)benzene 
• 107-05-1 3-chloroprop-1-ene 
• 106-95-6 allyl bromide 
• 5162-44-7 1-bromo-4-butene 

Downstream Products

• 60333-69-9 Triethoxy-(3-o-bromphenoxypropyl)-silan 
• 13524-73-7 3-methyl-2,3-dihydrobenzofuran 
• 119488-14-1 3-(3-benzenesulfonylpropyl)-2,3-dihydrobenzofuran 
• 1746-13-0 allyl phenyl ether 
• 108-95-2 phenol 
• 417710-20-4 Ti(NC(CH₃)3C₆H₃(CH₃)2)3Br 
• 59086-52-1 2-allyloxybenzoic acid 
• 328125-38-8 2-(2,3-dihydrobenzofuran-3-yl)acetic acid 
• 38770-76-2 1-bromo-2-(prop-2-yn-1-yloxy)benzene 
• 852110-51-1 7-bromo-2-hydroxymethyl-2,3-dihydrobenzo[b]furan 
• 10292-60-1 2-cyclopropylphenol 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 179938-94-4 (Z)-1-bromo-2-(prop-1-en-1-yloxy)benzene 

Relevant articles and documents

THERAPEUTIC COMPOUNDS AND METHODS OF USE

The invention relates to compounds and methods of using said compounds, as well as pharmaceutical compositions containing such compounds, for treating diseases and conditions mediated by TEAD, such as cancer.

COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF PARASITIC DISEASES

The present invention provides a compound of formula (Ia) or a pharmaceutically acceptable salt thereof; a method for manufacturing the compounds of the invention, solid forms, combinations of pharmacologically active agents, pharmaceutical compositions and methods of using such compounds and solid forms thereof to treat or prevent parasitic diseases, for example malaria.

Synthesis of All-Carbon Quaternary Centers by Palladium-Catalyzed Olefin Dicarbofunctionalization

The redox-neutral dicarbofunctionalization of tri- and tetrasubstituted olefins to form a variety of (hetero)cyclic compounds under photoinduced palladium catalysis is described. This cascade reaction process was used to couple styrenes or acryl amides with a broad range of highly decorated olefins tethered to aryl or alkyl bromides (>50 examples). This procedure enables one or two contiguous all-carbon quaternary centers to be formed in a single step. The products could be readily diversified and applied in the synthesis of a bioactive oxindole analogue.