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847470-39-7

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847470-39-7 Usage

Structure

1H-Benzimidazole derivative with a 4-iodophenyl substitution

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals

Biological activities

Antimicrobial and antifungal properties

Industry applications

Versatile chemical with potential applications in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 847470-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,4,7 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 847470-39:
(8*8)+(7*4)+(6*7)+(5*4)+(4*7)+(3*0)+(2*3)+(1*9)=197
197 % 10 = 7
So 847470-39-7 is a valid CAS Registry Number.

847470-39-7Upstream product

847470-39-7Downstream Products

847470-39-7Relevant articles and documents

Method used for rapid preparation of benzo-heterocycle compound with physical grinding under solvent-free room temperature conditions

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Paragraph 0018; 0032, (2019/01/21)

The invention discloses a method used for rapid preparation of benzo-heterocycle compound with physical grinding under solvent-free room temperature conditions. According to the method, glacial aceticacid is taken as a catalyst; at solvent-free room temperature conditions, physical grinding is adopted, reaction of 2-substituted arylamines (2-mercapto arylamine, 2-aminophenol, and o-phenylenediamine) and aromatic aldehydes is carried out using physical grinding. The method is friendly to the environment, is simple in operation, is safe, is low in cost, and is high in efficiency. Compared withthe prior art, the advantages are that: the method is suitable for a large amount of functional groups, yield is high, less by-product is generated, operation is simple, the method is safe, cost is low, and the method is friendly to the environment.

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