2-(Piperidin-2-ylmethyl)-3,3,3-trifluoropropanoic acid

off-white powder

Reagent Code: #43873
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CAS Number 480438-80-0

science Other reagents with same CAS 480438-80-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.21 g/mol
Formula C₉H₁₄F₃NO₂
badge Registry Numbers
MDL Number MFCD03427205
thermostat Physical Properties
Melting Point 133-137℃(lit.)
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring and trifluoromethyl group, makes it valuable for developing drugs targeting neurological disorders, such as Alzheimer's disease and depression. Additionally, it is explored in the creation of enzyme inhibitors and receptor modulators due to its ability to interact with biological targets effectively. Its trifluoromethyl group enhances metabolic stability, making it a promising candidate for improving drug efficacy and pharmacokinetics.

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inventory 1g
10-20 days ฿17,505.00

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2-(Piperidin-2-ylmethyl)-3,3,3-trifluoropropanoic acid
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring and trifluoromethyl group, makes it valuable for developing drugs targeting neurological disorders, such as Alzheimer's disease and depression. Additionally, it is explored in the creation of enzyme inhibitors and receptor modulators due to its ability to interact with biological targets effectively. Its trifluoromethyl group enh

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring and trifluoromethyl group, makes it valuable for developing drugs targeting neurological disorders, such as Alzheimer's disease and depression. Additionally, it is explored in the creation of enzyme inhibitors and receptor modulators due to its ability to interact with biological targets effectively. Its trifluoromethyl group enhances metabolic stability, making it a promising candidate for improving drug efficacy and pharmacokinetics.

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