CAS 23623-06-5

2,5'-Bi-1H-benzimidazole,2'-(4-methoxyphenyl)-5-(4-methyl-1-piperazinyl)- (9CI)

Description:

2,5'-Bi-1H-benzimidazole, 2'-(4-methoxyphenyl)-5-(4-methyl-1-piperazinyl)-, with the CAS number 23623-06-5, is a chemical compound characterized by its complex structure, which includes a bi-benzimidazole core and substituents that enhance its pharmacological properties. This compound features a methoxyphenyl group and a piperazinyl moiety, which contribute to its potential biological activity. The presence of the piperazine ring suggests possible interactions with neurotransmitter receptors, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting central nervous system disorders. The compound is likely to exhibit moderate to high solubility in organic solvents, and its stability can be influenced by environmental factors such as pH and temperature. Additionally, the presence of multiple functional groups may allow for various chemical modifications, enhancing its versatility in research and application. Overall, this compound represents a significant interest in the field of drug discovery and development due to its structural features and potential therapeutic implications.

Formula: C₂₆H₂₆N₆O

Synonyms:

• 2,5'-Bibenzimidazole,2'-(p-methoxyphenyl)-5-(4-methyl-1-piperazinyl)- (8CI)
• 2-[2-(4-Methoxyphenyl)-6-benzimidazolyl]-6-(1-methyl-4-piperazinyl)benzimidazole
• Hoe 32021

HOE-32021

CAS: 23623-06-5

Formula: C₂₆H₂₆N₆O

Purity: 95%

Molecular weight: 438.5242

Ref: IN-DA00BF3M

HOE 32021

CAS: 23623-06-5

HOE 32021

Purity: ≥98%

Molecular weight: 438.52g/mol

Ref: 54-BUP17459

HOE 32021

CAS: 23623-06-5

HOE 32021 is an intracellular DNA dye that binds to nucleic acids by intercalating in the minor groove of DNA duplexes.

Formula: C₂₆H₂₆N₆O

Purity: 99.02%

Color and Shape: Solid

Molecular weight: 438.52

Ref: TM-T15496

HOE 32021

CAS: 23623-06-5

HOE 32021 is a fungicide, which is developed from synthetic chemical sources with a broad spectrum mode of action. As a multisite inhibitor, it targets several pathways crucial for fungal survival, effectively impeding spore germination and mycelial growth. This mode of action reduces the likelihood of resistance development among targeted pathogens.

Formula: C₂₆H₂₆N₆O

Purity: Min. 95%

Molecular weight: 438.52 g/mol

Ref: 3D-YAA62306