4857-05-0 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
Describes the physical appearance of the compound in its pure form.
Explanation
Indicates that the compound is capable of dissolving other substances, making it useful in a range of applications.
Explanation
The compound has properties that prevent freezing, making it suitable for use in antifreeze formulations.
Explanation
The compound has been studied for its possible uses in these industries, suggesting it may have beneficial properties or effects.
Explanation
The systematic name is a standardized way of naming the compound, used in scientific literature and databases for identification purposes.
Explanation
The compound's structure consists of a benzimidazole ring attached to an ethane diol group, which contributes to its properties and applications.
Explanation
The compound is classified as an organic compound, meaning it primarily consists of carbon and hydrogen atoms.
Explanation
The compound is in a liquid state under normal environmental conditions, which affects its handling and use in various applications.
Explanation
The material provided does not specify any hazardous properties, but
Appearance
Clear, colorless liquid
Solvent
Used in various industrial processes
Antifreeze properties
Used in the production of antifreeze agents
Potential applications
Pharmaceutical and agricultural industries
Chemical structure
Contains a benzimidazole ring and an ethane diol group
Chemical class
Organic compound
Physical state
Liquid at room temperature
Hazardous properties
Unknown
Check Digit Verification of cas no
The CAS Registry Mumber 4857-05-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4857-05:
(6*4)+(5*8)+(4*5)+(3*7)+(2*0)+(1*5)=110
110 % 10 = 0
So 4857-05-0 is a valid CAS Registry Number.
4857-05-0Relevant articles and documents
Gold catalysis opens up a new route for the synthesis of benzimidazoylquinoxaline derivatives from biomass-derived products (glycerol)
Climent, Maria J.,Corma, Avelino,Iborra, Sara,Martinez-Silvestre, Sergio
, p. 3866 - 3874 (2014/01/06)
Process intensification by using well-defined solid catalysts able to perform one-pot multistep reactions is one of the open fronts in heterogeneous catalysis. This is even more relevant if new, more efficient synthesis routes are open. Herein, a gold catalyst was used to synthesize benzimidazoylquinoxalines compounds by two efficient and selective novel methods in a multistep one-pot methodology. The first method involved the synthesis of benzimidazoylquinoxaline compounds with the same substituents in both heterocycles through oxidation-cyclization of glycerol with o-phenylenediamine derivatives, whereas the second one allowed the synthesis of benzimidazoylquinoxalines compounds with different substituents in each aromatic ring through coupling of o-phenylenediamine derivatives with glyceraldehyde in a first stage to produce the benzimidazol compound as an intermediate, followed by an oxidation-cyclization with another o-phenylenediamine compound in a second stage. Both stages were performed by using gold nanoparticles supported on nanoparticulated ceria (Au/CeO2) as the catalyst and air as the oxidant, in absence of any homogeneous reagent. A reaction mechanism has been proposed. A smooth route: Benzimidazoylquinoxaline derivatives can be obtained in good yields through one-pot oxidative coupling of glycerol or glyceraldehydes with 1,2-phenylenediamines in a two-step reaction, using Au/CeO2 as the catalyst, base-free conditions, mild temperature, and air as the oxidant. Copyright
