1-(Piperidin-4-yl)-5-(trifluoromethyl)-1H-benzo[d][1,2,3]triazole hydrochloride

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Reagent Code: #227577
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CAS Number 306935-37-5

science Other reagents with same CAS 306935-37-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.72 g/mol
Formula C₁₂H₁₄ClF₃N₄
badge Registry Numbers
MDL Number MFCD01566553
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds. Its structure supports the development of central nervous system agents, particularly serotonin and dopamine receptor modulators. The compound’s trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for improved brain penetration. It is also employed in the preparation of selective enzyme inhibitors and has been explored in the context of antipsychotic and antidepressant drug design. Due to its piperidine-benzotriazole framework, it serves as a scaffold in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,390.00
inventory 250mg
10-20 days ฿5,480.00
inventory 1g
10-20 days ฿19,210.00

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1-(Piperidin-4-yl)-5-(trifluoromethyl)-1H-benzo[d][1,2,3]triazole hydrochloride
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Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds. Its structure supports the development of central nervous system agents, particularly serotonin and dopamine receptor modulators. The compound’s trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for improved brain penetration. It is also employed in the preparation of selective enzyme inhibitors and has been explored in the

Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds. Its structure supports the development of central nervous system agents, particularly serotonin and dopamine receptor modulators. The compound’s trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in optimizing drug candidates for improved brain penetration. It is also employed in the preparation of selective enzyme inhibitors and has been explored in the context of antipsychotic and antidepressant drug design. Due to its piperidine-benzotriazole framework, it serves as a scaffold in medicinal chemistry for structure-activity relationship studies.

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