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1,4-Phenylenebis(methylene) bis(2-bromoacetate) is a chemical compound with the molecular formula C10H10Br2O4. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 1,4-phenylenebis(methylene) bis(2-bromoacetate) is a bis-ester derivative of 1,4-phenylenebis(methylene), where each methylene group is substituted with a 2-bromoacetate group. It is often used as a monomer in the synthesis of various polymers, particularly in the production of polyamides and polyesters. Due to the presence of bromine atoms, it can also be used in flame-retardant applications. The compound is synthesized through the reaction of 1,4-phenylenediamine with 2-bromoacetyl bromide. It is important to handle 1,4-phenylenebis(methylene) bis(2-bromoacetate) with care due to its potential toxicity and reactivity with nucleophiles.

34596-26-4

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34596-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34596-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,9 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34596-26:
(7*3)+(6*4)+(5*5)+(4*9)+(3*6)+(2*2)+(1*6)=134
134 % 10 = 4
So 34596-26-4 is a valid CAS Registry Number.

34596-26-4Downstream Products

34596-26-4Relevant academic research and scientific papers

Click synthesis of some mono/bis 1,2,3-triazoles with ester linkage and their microbicidal activity

Kaushik,Pahwa, Ashima

, p. 2171 - 2176 (2017)

Synthesis of some new 1,4-disubstituted 1,2,3-triazoles with ester functionality is reported employing Cu(I) catalyzed Huisgen [3+2] cycloaddition reaction of prop-2-yn-1-yl benzoates with 1,4-phenylenebis(methylene) bis(2-azidoacetate) and benzyl 2-azidoacetates. The synthesized compounds were well characterized through FTIR, 1H NMR, 13C NMR and HRMS. Further, the synthesized triazole derivatives were accessed for in vitro antimicrobial activity against one Gram-positive bacterial strain Staphylococcus aureus, three Gram-negative bacterial strains Escherichia coli, Klebsiella pneumoniae, Enterobacter aerogenes and two fungi Candida albicans and Aspergillus niger. Few of the synthesized disubstituted 1,2,3-triazoles displayed moderate to good inhibitory activity against tested microbial strains.

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