175844-47-0

Usage

Derivative

Benzene

Attached atoms

Two bromine atoms and two methoxy groups

Usage

Organic synthesis and building block in pharmaceuticals and agrochemicals production

Physical state

White to off-white solid

Molecular weight

285.96 g/mol

Melting point

Around 68-70°C

Flammability

Flammable

Health hazards

Potential health hazards, should be handled with care

Upstream product

• 91-16-7 1,2-dimethoxybenzene 

Downstream Products

• 852547-27-4 C₁₃H₇Br₅O₄ 
• 1254068-16-0 N-(4-bromo-2,3-dimethoxyphenethyl)-2-(3,4-dimethoxyphenyl)acetamide 
• 1411714-51-6 C₃₀H₃₁NO₅ 
• 1411714-55-0 C₃₀H₂₇NO₄ 
• 1254068-17-1 N-[4-(4-biphenyl)-2,3-dimethoxyphenethyl]-2-(3,4-dimethoxyphenyl)acetamide 
• 1310109-73-9 C₃₂H₃₁NO₄ 
• 1254068-18-2 7-(biphenyl-4-yl)-1-(3,4-dimethoxybenzyl)-5,6-dimethoxyisoquinoline 
• 1411714-40-3 C₃₀H₃₇NO₅ 
• 1254068-15-9 2-(4-bromo-2,3-dimethoxyphenyl)ethanamine 
• 1411714-46-9 C₃₀H₃₃NO₄ 
• 1411714-47-0 C₂₆H₂₉NO₅ 
• 1411714-49-2 C₂₆H₂₅NO₄ 
• 1254068-14-8 1-bromo-2,3-dimethoxy-4-(2-nitroethyl)benzene 
• 1411713-83-1 C₃₆H₃₄NO₄⁽¹⁺⁾ 

Relevant academic research and scientific papers

Topology-Guided Stepwise Insertion of Three Secondary Linkers in Zirconium Metal-Organic Frameworks

We report a topology-guided, precise insertion of three distinct secondary linkers into a zirconium-based metal-organic framework, NPF-300. Constructed from a tetratopic linker L and Zr6 cluster, NPP-300 exhibits a unique scu topology and certain flexibility along the crystallographic a axis, and in conjunction with the conformation change of the primary ligand, is able to accommodate the stepwise insertion of three different secondary linkers along the a and c axes. Size-matching and mechanic strain of the resulting framework are two important factors that determine the chemical stability of the inserted linkers. Secondary linker insertion in NPF-300 significantly enables not only its porosity but also potentials to install up to three different functional groups for the construction of multivariate MOFs with homogeneity.

Antibacterial activity of substituted dibenzo[a,g]quinolizin-7-ium derivatives

Berberine is a substituted dibenzo[a,g]quinolizin-7-ium derivative whose modest antibiotic activity is derived from its disruptive impact on the function of the essential bacterial cell division protein FtsZ. The present study reveals that the presence of

ANTIMICROBIAL AGENTS

The invention provides a compound of formula (I): or a salt or prodrug thereof, wherein Y, W, Z, Z1, Z2, Z3, Z4, and R1- R12 have any of the values described in the specification, as well as compositions comprising a compound of formula (I). The compounds are useful as antibacterial agents

PROCESS FOR THE PREPARATION OF GUANIDINO SUBSTITUTED BI-AND POLYPHENYLS THAT ARE SUITABLE AS SMALL MOLECULE CARRIERS

A process for the production of a compound of formula (I), or a pharmaceutically acceptable salt thereof, Formula (I) which process comprises:(a) coupling a compound of formula (II) to a compound of formula (III) to form a compound of formula (IV).

Synthesis of linear oligo(catechol) ligands for the metal directed self-assembling of helicates

The synthesis of the oligo(catechol) systems 1-4 with different substituents, length of the connecting spacer, and number of catechol units is achieved by the use of various coupling reactions (e.g. Wurtz, Glaser-Eglinton, Stephens-Castro). In order to do this methods of preparing the building blocks, 2,3-dimethoxybenzyl bromides 5, 2,3-dimethoxyphenylacetylene (17), or 1,4-dibromo-2,3-dimethoxybenzene (23) have been developed starting with simple catechol (benzene-1,2-diol) derivatives.