1-(3-(Dimethylamino)propyl)-1-(4-fluorophenyl)-3-hydroxy-1,3-dihydroisobenzofuran-5-carbonitrile oxalate

95%

Reagent Code: #167717
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CAS Number 1332724-03-4

science Other reagents with same CAS 1332724-03-4

blur_circular Chemical Specifications

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Weight 430.43 g/mol
Formula C₂₂H₂₃FN₂O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs). Its structure supports the creation of bioactive molecules with central nervous system activity. Commonly employed in research settings for optimizing drug candidates targeting depression and anxiety disorders. Also utilized in analytical studies to understand metabolic pathways and drug interactions due to its functional groups and stability under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿110,110.00

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1-(3-(Dimethylamino)propyl)-1-(4-fluorophenyl)-3-hydroxy-1,3-dihydroisobenzofuran-5-carbonitrile oxalate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs). Its structure supports the creation of bioactive molecules with central nervous system activity. Commonly employed in research settings for optimizing drug candidates targeting depression and anxiety disorders. Also utilized in analytical studies to understand metabolic pathways and drug interactions due to its functional groups and stability under vari

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs). Its structure supports the creation of bioactive molecules with central nervous system activity. Commonly employed in research settings for optimizing drug candidates targeting depression and anxiety disorders. Also utilized in analytical studies to understand metabolic pathways and drug interactions due to its functional groups and stability under various reaction conditions.

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