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72572-18-0

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72572-18-0 Usage

Chemical Family

1H-Benzimidazole, 5-ethyl-(9CI) belongs to the benzimidazole family, which is a group of heterocyclic compounds.

Bicyclic Structure

The benzimidazole family is characterized by a bicyclic structure, which means that the compounds have two rings of atoms in their structure.

Ethyl Group

The presence of an ethyl group at the 5-position of the benzimidazole ring gives the compound its specific properties and potential applications.

Biological Activities

Benzimidazoles have been linked to various biological activities, including antimicrobial, antiviral, and anticancer effects.

Pharmaceutical Research

As a result of their potential biological activities, 1H-Benzimidazole, 5-ethyl-(9CI) could be of interest in pharmaceutical research and drug development.

Potential Applications

The chemical structure and properties of 1H-Benzimidazole, 5-ethyl-(9CI) make it a potentially valuable compound for further study and potential applications in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 72572-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,7 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72572-18:
(7*7)+(6*2)+(5*5)+(4*7)+(3*2)+(2*1)+(1*8)=130
130 % 10 = 0
So 72572-18-0 is a valid CAS Registry Number.

72572-18-0Downstream Products

72572-18-0Relevant articles and documents

Microwave use of amidine compounds in the aqueous phase benzoate synthesis of benzimidazole compounds method

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Paragraph 0081, (2019/03/28)

The invention discloses a microwave the use of amidine compounds in the aqueous phase benzoate synthesis of benzimidazole compounds, in the aqueous phase under microwave conditions adding benzoic amidine compound under alkaline condition [...] into benzimidazole reaction, invention an environment-friendly, the operation is simple, cheap and safe, efficient process for preparing benzimidazole method. Compared with the prior art, this method not only can be applied to a large number of functional groups, the productive rate is high, few by-products, and the operation is simple, safe, low cost, environmental protection; .

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