(S)-3-Amino-3-cyclohexylpropanoic acid

95%

Reagent Code: #57170
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CAS Number 91383-14-1

science Other reagents with same CAS 91383-14-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.24 g/mol
Formula C₉H₁₇NO₂
badge Registry Numbers
MDL Number MFCD07373036
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

(S)-3-Amino-3-cyclohexylpropanoic acid is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting neurological and metabolic disorders. Its structure allows it to act as a building block for designing molecules that can interact with specific biological targets, such as enzymes or receptors. In research, it is often employed to develop peptide analogs and other bioactive molecules due to its chiral center, which can influence the stereochemistry and efficacy of the final drug. Additionally, it has been explored in the creation of inhibitors for enzymes involved in disease pathways, making it valuable for therapeutic applications. Its cyclohexyl group contributes to the stability and lipophilicity of the resulting compounds, enhancing their potential as drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,629.00
inventory 250mg
10-20 days ฿2,439.00
inventory 1g
10-20 days ฿6,912.00

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(S)-3-Amino-3-cyclohexylpropanoic acid
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(S)-3-Amino-3-cyclohexylpropanoic acid is primarily used in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical compounds, particularly those targeting neurological and metabolic disorders. Its structure allows it to act as a building block for designing molecules that can interact with specific biological targets, such as enzymes or receptors. In research, it is often employed to develop peptide analogs and other bioactive molecules due to its chiral center, which can influence the stereochemistry and efficacy of the final drug. Additionally, it has been explored in the creation of inhibitors for enzymes involved in disease pathways, making it valuable for therapeutic applications. Its cyclohexyl group contributes to the stability and lipophilicity of the resulting compounds, enhancing their potential as drug candidates.
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