1020991-05-2

Basic information

• Product Name: 2-bromo-4-methyl-1-(prop-2-yn-1-yloxy)benzene
• Synonyms: 2-bromo-4-methyl-1-(prop-2-yn-1-yloxy)benzene
• CAS NO: 1020991-05-2
• Molecular Weight: 225.085
• Mol File: 1020991-05-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-bromo-4-methyl-1-(prop-2-yn-1-yloxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-4-methyl-1-(prop-2-yn-1-yloxy)benzene(1020991-05-2)
• EPA Substance Registry System: 2-bromo-4-methyl-1-(prop-2-yn-1-yloxy)benzene(1020991-05-2)

Safety Data

• Hazardous Substances Data: 1020991-05-2(Hazardous Substances Data)

Upstream product

• 6627-55-0 2-bromo-p-cresol 
• 106-96-7 propargyl bromide 

Downstream Products

• 1384484-62-1 1,6-bis(2-bromo-4-methylphenoxy)-2,4-hexadiyne 
• 1431465-19-8 (Z)-3-((4-methoxyphenyl)(phenyl)-methylene)-5-methyl-2,3-dihydrobenzofuran 
• 1431465-30-3 C₂₃H₂₀O₂ 
• 1431465-20-1 3-(bis(4-methoxyphenyl)methylene)-5-methyl-2,3-dihydrobenzofuran 
• 1431465-21-2 (Z)-methyl 4-((4-methoxyphenyl)(5-methylbenzofuran-3(2H)-ylidene)methyl)benzoate 
• 1431465-22-3 (E)-methyl 3-((4-methoxyphenyl)(5-methylbenzofuran-3(2H)-ylidene)methyl)benzoate 
• 1431465-23-4 (E)-3-((4-methoxyphenyl)(5-methylbenzofuran-3(2H)-ylidene)methyl)benzaldehyde 
• 1431465-24-5 (Z)-1-(4-((5-methylbenzofuran-3(2H)-ylidene)(phenyl)methyl)phenyl)ethanone 
• 1431465-25-6 (E)-1-(4-((4-methoxyphenyl)(5-methylbenzofuran-3(2H)-ylidene)-methyl)phenyl)ethanone 
• 1431465-26-7 (E)-methyl 4-((4-acetylphenyl)(5-methylbenzofuran-3(2H)-ylidene)methyl)benzoate 
• 1431465-27-8 (E)-methyl 3-((4-acetylphenyl)(5-methylbenzofuran-3(2H)-ylidene)methyl)benzoate 
• 1431465-28-9 (E)-3-((4-acetylphenyl)(5-methylbenzofuran-3(2H)-ylidene)methyl)benzaldehyde 
• 1431465-29-0 3-(diphenylmethylene)-5-methyl-2,3-dihydrobenzofuran 
• 1431465-45-0 (E)-3-((4-methoxyphenyl)(phenyl)methylene)-5-methyl-2,3-dihydrobenzofuran 

Relevant articles and documents

A convenient method for the synthesis of (prop-2-ynyloxy)benzene derivatives via reaction with propargyl bromide, their optimization, scope and biological evaluation

A highly convenient method has been developed for the synthesis of (prop-2-ynyloxy) benzene and its derivatives. Differently substituted phenol and aniline derivatives were allowed to react with propargyl bromide in the presence of K2CO3/

Isopropanol and potassium tert-butoxide promoted intramolecular direct sp2 C-H functionalization: An expedient synthesis of 1,2,3-triazole annulated chromens and quinolones

A series of 1,2,3-triazole annulated chromen and quinolone derivatives have been synthesized by means of direct sp2 C-H functionalization in the presence of iso-propanol and potassium tert-butoxide. The reaction proceeds through homolytic aroma

Hybrid system of metal/Bronsted acid relay catalysis for the intramolecular double hydroarylation and cationic cyclization of diyne diethers and diamines

We have developed a hybrid system of metal/Bronsted acid relay catalysis for the intramolecular double hydroarylation and cationic cyclization of diyne diethers and diamines to give 4,4′-bi(2H-chromene), bi(2H-quinoline), and dioxafluoranthenes starting f