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153407-10-4

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153407-10-4 Usage

Usage in research

Organic synthesis and medicinal chemistry 1-methoxymethoxy-4-(4-bromophenyl)benzene is commonly used in these fields to study organic reactions and develop pharmaceutical drugs.

Applications in pharmaceutical drug development

The compound has significant applications in creating new drugs, potentially leading to the discovery of new treatments and therapies.

Building block for novel materials

The compound has potential uses as a building block for creating new materials, which could have various applications in different industries.

Precursor for synthesis of functional molecules

1-methoxymethoxy-4-(4-bromophenyl)benzene can be used as a starting material for the synthesis of various functional molecules, expanding its utility in chemical and pharmaceutical research.

Valuable properties

The compound possesses interesting and valuable properties that make it a valuable compound in the fields of chemistry and pharmaceutical science, although specific properties are not mentioned in the provided material.

Check Digit Verification of cas no

The CAS Registry Mumber 153407-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,4,0 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153407-10:
(8*1)+(7*5)+(6*3)+(5*4)+(4*0)+(3*7)+(2*1)+(1*0)=104
104 % 10 = 4
So 153407-10-4 is a valid CAS Registry Number.

153407-10-4Relevant articles and documents

Supramolecular polymer chemistry: Design, synthesis, characterization, and kinetics, thermodynamics, and fidelity of formation of self-assembled dendrimers

Zeng, Fanwen,Zimmerman, Steven C,Kolotuchin, Sergei V,Reichert, David E.C,Ma, Yuguo

, p. 825 - 843 (2007/10/03)

Dendrimers 1a-d were synthesized in 10 steps from dendrons 4-7, bromobenzene and succinic anhydride. Tetraacids 1e and 1f were prepared in an analogous fashion. The aggregation of 1a-f was studied in solution by size exclusion chromatography (SEC), vapor pressure osmometry (VPO), low angle laser light scattering (LLS), small angle neutron scattering (SANS), and by 1H NMR. The data are consistent with a stable, discrete hexameric aggregate for 1b-d in methylene chloride, non-discrete polymeric aggregates for 1a, 1e, and 1f, and monomers for all compounds in tetrahydrofuran and dimethyl sulfoxide. Kinetic and thermodynamic studies and mixing experiments confirmed the highly cooperative nature of the self-assembly process.

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