5847-89-2 Usage
General Description
1H-Benzimidazole, 4-fluoro- is a chemical compound that belongs to the benzimidazole family. It is a derivative of benzimidazole with a fluorine atom attached to the fourth position of the molecule. 1H-BENZIMIDAZOLE, 4-FLUORO- has been studied for its potential pharmaceutical applications, particularly in the field of medicinal chemistry. It is known to exhibit biological activity and has been investigated for its potential use as a drug candidate in the treatment of various diseases. Its structure and properties make it a promising candidate for further research and development in the field of drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 5847-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5847-89:
(6*5)+(5*8)+(4*4)+(3*7)+(2*8)+(1*9)=132
132 % 10 = 2
So 5847-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H11Cl2NO/c18-15-7-3-6-14(16(15)19)17(21)20-13-9-8-11-4-1-2-5-12(11)10-13/h1-10H,(H,20,21)
5847-89-2Relevant articles and documents
Microwave use of amidine compounds in the aqueous phase benzoate synthesis of benzimidazole compounds method
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Paragraph 0068, (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; .
The synthesis of some fluoronitrobenzimidazoles and their reactivities toward peptide nucleophiles.
Kirk,Cohen
, p. 384 - 389 (2007/10/07)
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