40992-09-4

Basic information

• Product Name: 2-Methoxy-4-bromo-5-methylphenol
• Synonyms: 2-Methoxy-4-bromo-5-methylphenol;4-Bromo-2-methoxy-5-methylphenol
• CAS NO: 40992-09-4
• Molecular Formula: C₈H₉BrO₂
• Molecular Weight: 0
• Mol File: 40992-09-4.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Methoxy-4-bromo-5-methylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methoxy-4-bromo-5-methylphenol(40992-09-4)
• EPA Substance Registry System: 2-Methoxy-4-bromo-5-methylphenol(40992-09-4)

Safety Data

• Hazardous Substances Data: 40992-09-4(Hazardous Substances Data)

Upstream product

• 1195-09-1 5-methyl-2-methoxyphenol 
• 621-59-0 isovanillin 

Downstream Products

• 302321-76-2 4-bromo-6,6-dimethoxy-3-methyl-2,4-cyclohexadien-1-one 
• 486413-44-9 2-methoxy-5-methyl-4-trimethylsilanyl-phenol 
• 1453107-64-6 2,4,6-tris(4-((tert-butyldimethylsilyl)oxy)-5-methoxy-2-methylphenyl)-1,3,5,2,4,6-trioxatriborinane 
• 1453107-63-5 (4-bromo-2-methoxy-5-methylphenoxy)(tert-butyl)dimethylsilane 

Relevant articles and documents

INDOLINE DERIVATIVES

Compounds of Formula (I) are disclosed and methods of treating viral infections with compositions comprising such compounds.

Concise synthesis of the Hasubanan Alkaloid (±)-cepharatine A using a Suzuki coupling reaction to effect o,p -phenolic coupling

Suzuki coupling of 10 and 11 resulted in 9, which was O-alkylated to provide 12. Treatment of 12 with CsF in DMF resulted in the formation of the completed core structure 13 in a single step. Reductive amination of 13 completed the synthesis of (±)-cepharatine A, 4.

A new and highly stereoselective approach to cis-clerodanes

A new and highly stereoselective approach to cis-clerodanes and its application to the synthesis of (±)-2 is described.