58442-17-4

Usage

Uses

Used in Pharmaceutical Industry:
1H-Benzimidazole-5-carboxaldehyde 97+% is used as a key intermediate for the synthesis of various pharmaceutical compounds with potential therapeutic applications. Its unique structure and reactivity enable the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 1H-Benzimidazole-5-carboxaldehyde 97+% is utilized as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its versatility in chemical reactions allows for the creation of novel compounds with enhanced performance and selectivity in agricultural applications.
Used in Organic Synthesis Research:
1H-Benzimidazole-5-carboxaldehyde 97+% is employed as a valuable building block in organic synthesis research, where its high purity and reactivity are crucial for the development of new synthetic routes and the exploration of novel chemical reactions. 1H-BENZIMIDAZOLE-5-CARBOXALDEHYDE 97+%'s properties make it an ideal candidate for the synthesis of complex organic molecules and the investigation of their properties and potential applications.
Used in the Synthesis of Heterocyclic Compounds:
1H-Benzimidazole-5-carboxaldehyde 97+% is used as a starting material in the production of various heterocyclic compounds, which are important in numerous fields, including pharmaceuticals, materials science, and agrochemicals. The high purity of 1H-BENZIMIDAZOLE-5-CARBOXALDEHYDE 97+% ensures the quality and consistency of the synthesized heterocyclic compounds, facilitating their use in various applications.

InChI:InChI=1/C8H6N2O/c11-4-6-1-2-7-8(3-6)10-5-9-7/h1-5H,(H,9,10)

Upstream product

• 75-09-2 dichloromethane 
• 7529-22-8 4-methylmorpholine N-oxide 
• 15788-16-6 5-benzimidazolecarboxylic acid 

Downstream Products

• 181867-19-6 1-methyl-1H-benzo[d]imidazole-6-carbaldehyde 
• 279226-70-9 1-methyl-1H-benzo[d]imidazole-5-carbaldehyde 
• 1342888-82-7 N-((1H-Benzo[d]imidazol-5-yl)methyl)benzenamine 
• 5918-89-8 N-benzyl-1H-benzo[d]imidazol-5-amine 
• 1072121-67-5 (Z)-5-[2-(3,5-dimethoxyphenyl)-ethenyl]-1H-benzoimidazole 
• 865878-73-5 1H-benzo[d]imidazole-5-formaldehyde oxime 

Relevant academic research and scientific papers

Trisbenzimidazoles useful as topoisomerase I inhibitors

The present invention provides anti-neoplastic topoisomerase I inhibitors of the formula: STR1 wherein Ar is (C6 -C12)aryl or (5- to 12-membered) heteroaryl comprising 1-3 N, S or non-peroxide O, wherein N is unsubstituted or is substituted with (C1 -C4)alkyl; X is H, CN, CHO, OH, acetyl, CF3, O(C1 -C4)alkyl, NO2, NH2, halogen or halo-(C1 -C4)alkyl; each Y is individually H, (C1 -C4)alkyl or aralkyl; Y' is H or (C1 -C4)alkyl; n is 0 or 1; and each Z is individually H, (C1 -C4)alkyl, halogen or halo(C1 -C4)alkyl; or a pharmaceutically acceptable salt therein.

Terbenzimidazoles useful as antifungal agents

The present invention provides a method of treatment of fungal infection with an antifungal topoisomerase I inhibitor of the formula: STR1 wherein Ar is (C6 -C12)aryl, a (5- to 12-membered) heteroaryl comprising 1-3 N, S or non-peroxide O, wherein N is unsubstituted or is substituted with H, (C1 -C4)alkyl or benzyl; or benzo; X is H, CN, CHO, OH, acetyl, CF3, O(C1 -C4)alkyl, NO2, NH2, halogen or halo-(C1 -C4)alkyl; each Y is individually H, (C1 -C4)alkyl or aralkyl; Y' is H or (C1 -C4)alkyl; n is 0 or 1; and each Z is individually H, (C1 -C4)alkyl, halogen or halo(C1 -C4)alkyl; or a pharmaceutically acceptable salt thereof.