121449-70-5

Basic information

• Product Name: Phenol, 2-bromo-3,5-dimethoxy-
• CAS NO: 121449-70-5
• Molecular Formula: C8H9BrO3
• Molecular Weight: 233.062
• Mol File: 121449-70-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Phenol, 2-bromo-3,5-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-bromo-3,5-dimethoxy-(121449-70-5)
• EPA Substance Registry System: Phenol, 2-bromo-3,5-dimethoxy-(121449-70-5)

Safety Data

• Hazardous Substances Data: 121449-70-5(Hazardous Substances Data)

Upstream product

• 500-99-2 3,5-dimethoxyphenol 
• 316140-47-3 1-acetoxy-2-bromo-3,5-dimethoxy-benzene 
• 23133-74-6 1-acetoxy-3,5-dimethoxy-benzene 

Downstream Products

• 316140-47-3 1-acetoxy-2-bromo-3,5-dimethoxy-benzene 
• 857561-40-1 1-(3-bromo-2-hydroxy-4,6-dimethoxy-phenyl)-2-chloro-ethanone 
• 47610-28-6 1-<2-Brom-3.5-dimethoxy-phenoxy>-4-benzyloxy-cyclohexan-carbonsaeure-(1) 
• 92582-73-5 1-<2-Brom-3.5-dimethoxy-phenoxy>-cyclohexan-carbonsaeure-(1) 
• 316140-43-9 (2'S)-(-)-1'-fluorooct-7'-en-2'-yl 2,4-dimethoxy-6-trifluoromethanesulfonatebenzoate 
• 316140-41-7 1'-fluorooct-7'-en-2'-yl 2,4-dimethoxy-6-trifluoromethanesulfonatebenzoate 
• 316140-34-8 1'-fluorooct-7'-en-2'-yl 2-allyl-4,6-dimethoxybenzoate 
• 316140-44-0 (2'S)-(-)-1'-fluorooct-7'-en-2'-yl 2-allyl-4,6-dimethoxybenzoate 
• 316140-35-9 1'-fluorooct-7'-en-2'-yl 2-hydroxy-4,6-dimethoxybenzoate 
• 316140-42-8 (2'S)-(-)-1'-fluorooct-7'-en-2'-yl 2-hydroxy-4,6-dimethoxybenzoate 
• 3187-19-7 2,4-dimethoxysalicylic acid 
• 487-06-9 Limettin 
• 129103-80-6 Benzoic acid 2-bromo-3,5-dimethoxy-phenyl ester 

Relevant articles and documents

A Three-Phase Four-Component Coupling Reaction: Selective Synthesis of o-Chloro Benzoates by KCl, Arynes, CO2, and Chloroalkanes

A transition-metal-free three-phase four-component coupling reaction (3P-4CR) involving KCl, arynes, chloroalkanes and CO2 has been reported for the first time, enabling the incorporation of both chloro and CO2 into an aryne simultaneously. The reactions for the synthesis of different types of o-chloro benzoates can be selectively modulated by the chloroalkane utilized. The corresponding products can be alternatively transformed for postsynthetic functionalizations conveniently.

An aryne route to cytosporone B and phomopsin C

The octaketide cytosporone B has been synthesized in six steps using 1,3,5-trihydroxybenzene as a starting material via aryne insertion reaction into a carbon-carbon σ-bond.

Structure of an anti-plasmin inhibitor, eckol, isolated from the brown alga Ecklonia kurome Okamura and inhibitory activities of its derivatives on plasma plasmin inhibitors

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