(4-benzoyl-1-phenyltetrahydro-1H-pyrrol-3-yl)(phenyl)methanone

≥90%

Reagent Code: #197804
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CAS Number 343374-86-7

science Other reagents with same CAS 343374-86-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.44 g/mol
Formula C₂₄H₂₁NO₂
badge Registry Numbers
MDL Number MFCD01568809
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents targeting neurological disorders. Its structure supports the development of compounds with activity against neurodegenerative diseases, particularly due to its ability to interact with central nervous system receptors. Commonly employed in research settings for designing inhibitors that modulate enzyme activity involved in neurotransmitter regulation. Also utilized in the preparation of photoprobes for studying receptor binding sites because of its photoaffinity labeling capabilities. Shows promise in medicinal chemistry for creating analogs with improved blood-brain barrier penetration.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿5,990.00

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(4-benzoyl-1-phenyltetrahydro-1H-pyrrol-3-yl)(phenyl)methanone
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Used as a key intermediate in the synthesis of pharmaceutical agents targeting neurological disorders. Its structure supports the development of compounds with activity against neurodegenerative diseases, particularly due to its ability to interact with central nervous system receptors. Commonly employed in research settings for designing inhibitors that modulate enzyme activity involved in neurotransmitter regulation. Also utilized in the preparation of photoprobes for studying receptor binding sites be

Used as a key intermediate in the synthesis of pharmaceutical agents targeting neurological disorders. Its structure supports the development of compounds with activity against neurodegenerative diseases, particularly due to its ability to interact with central nervous system receptors. Commonly employed in research settings for designing inhibitors that modulate enzyme activity involved in neurotransmitter regulation. Also utilized in the preparation of photoprobes for studying receptor binding sites because of its photoaffinity labeling capabilities. Shows promise in medicinal chemistry for creating analogs with improved blood-brain barrier penetration.

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