89795-49-3 Usage
Uses
Used in Pharmaceutical Industry:
2-FURAN-2-YL-1H-IMIDAZOLE is used as a key intermediate in the synthesis of various pharmaceuticals, notably clotrimazole, an antifungal medication. Its presence in these compounds contributes to their therapeutic effects against fungal infections.
Used in Agricultural Industry:
In the agricultural sector, 2-FURAN-2-YL-1H-IMIDAZOLE is utilized in the synthesis of pesticides and herbicides. Its incorporation enhances the effectiveness of these products in controlling pests and unwanted plant growth, thereby supporting crop protection and yield maintenance.
2-FURAN-2-YL-1H-IMIDAZOLE's multifaceted applications underscore its importance in both the pharmaceutical and agricultural fields, making 2-FURAN-2-YL-1H-IMIDAZOLE a chemical of significant value.
Check Digit Verification of cas no
The CAS Registry Mumber 89795-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,9 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89795-49:
(7*8)+(6*9)+(5*7)+(4*9)+(3*5)+(2*4)+(1*9)=213
213 % 10 = 3
So 89795-49-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O/c1-2-6(10-5-1)7-8-3-4-9-7/h1-5H,(H,8,9)
89795-49-3Relevant academic research and scientific papers
A convenient procedure for preparing hetarylamides and their analogs by dehydrogenation of the corresponding imidazoles
Aleksandrov,El'Chaninov
experimental part, p. 1024 - 1026 (2011/01/05)
Conditions of aromatization of 2-(2-hetaryl)imidazolines and their analogs with various dehydrogenating agents were examined. A new catalytic system, Pd/C-diphenyl oxide, was studied, and the optimal catalyst:imidazoline ratio ensuring formation of 2-substituted imidazoles in high yield was found.
2-Substituted imidazoles. 1. Reactions of 1-methyl-2-(2-furyl)imidazole with electrophiles
Stoyanov,El'chaninov,Simonov,Pozharskii
, p. 1168 - 1172 (2007/10/02)
1-Methyl-2-(2-furyl)imidazole has been synthesized. Electrophilic attack (bromination, nitration, formylation, acylation, and hydroxymethylation) occurs in most cases at the free α-position of the furan ring.
