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2-(4-BROMO-2,6-DIMETHYLPHENOXY)ACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

455887-97-5

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455887-97-5 Usage

Type of compound

Derivative of acetic acid

Contains

Bromine atom, dimethylphenoxy group

Common uses

Organic synthesis, building block for pharmaceuticals, agrochemicals, and specialty chemicals

Potential uses

Herbicide, growth regulator, fungicide

Mechanism of action

Interferes with growth and development of plants and fungi

Additional applications

Research and development for creation of new chemical entities with therapeutic or agricultural uses

Check Digit Verification of cas no

The CAS Registry Mumber 455887-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,5,8,8 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 455887-97:
(8*4)+(7*5)+(6*5)+(5*8)+(4*8)+(3*7)+(2*9)+(1*7)=215
215 % 10 = 5
So 455887-97-5 is a valid CAS Registry Number.

455887-97-5Downstream Products

455887-97-5Relevant academic research and scientific papers

Formation of calix[4]arenes with acyloxycarboxylate functions

Bauer, David,Stipurin, Sergej,K?ckerling, Martin,Mamat, Constantin

, (2020)

Calix[4]arenes are an exciting class of multifunctional compounds. Their ability to bind small molecules and ions actively makes them useful tools for many applications. While looking for a suitable chelating agent, a particular modification of the calix[4]arene led to an unexpected side reaction. In this work, we will describe the selective formation of the observed acyloxyacetate derivatives. The according yields can be regulated by controlling the water content of the solvent system. All new compounds were obtained in yields higher than 45percent and fully characterized by NMR, MS, EA, and X-ray crystallography. By performing and analyzing several reactions with different calix[4]arenes and monomeric derivatives, an explanation for the reaction mechanism was postulated. Further, we report on the modification of reaction conditions which were investigated to verify our findings’ veracity. In total, three acyloxyacetate derivatives were synthesized and characterized to support our conclusions.

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