(R)-1-((1H-Imidazol-4-yl)methyl)-3-benzyl-4-(thiophen-2-ylsulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile hydrochloride

97%

Reagent Code: #113429
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CAS Number 195981-08-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 526.0700000000001 g/mol
Formula C₂₅H₂₄ClN₅O₂S₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate or active pharmaceutical ingredient (API) in the synthesis of novel therapeutic agents. Its structure suggests potential activity in targeting specific receptors or enzymes, making it valuable for research in neurological or psychiatric disorders. The presence of the imidazole and benzodiazepine moieties indicates its potential use in designing compounds for anxiety, insomnia, or other central nervous system-related conditions. Additionally, the thiophene sulfonyl group may contribute to its binding affinity or pharmacokinetic properties, enhancing its efficacy in drug formulations. Researchers often explore derivatives of this compound to optimize its pharmacological profile for clinical applications.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿13,680.00
(R)-1-((1H-Imidazol-4-yl)methyl)-3-benzyl-4-(thiophen-2-ylsulfonyl)-2,3,4,5-tetrahydro-1H-benzo[e][1,4]diazepine-7-carbonitrile hydrochloride
This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate or active pharmaceutical ingredient (API) in the synthesis of novel therapeutic agents. Its structure suggests potential activity in targeting specific receptors or enzymes, making it valuable for research in neurological or psychiatric disorders. The presence of the imidazole and benzodiazepine moieties indicates its potential use in designing compounds for anxiety, insomnia, or other central nervous system-related conditions. Additionally, the thiophene sulfonyl group may contribute to its binding affinity or pharmacokinetic properties, enhancing its efficacy in drug formulations. Researchers often explore derivatives of this compound to optimize its pharmacological profile for clinical applications.
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