(S)-2-Amino-3-cyclohexylpropanoic acid hydrate

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Reagent Code: #38284
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CAS Number 307310-72-1

science Other reagents with same CAS 307310-72-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.25 g/mol
Formula C₉H₁₉NO₃
badge Registry Numbers
MDL Number MFCD03703498
thermostat Physical Properties
Boiling Point 387°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

(S)-2-Amino-3-cyclohexylpropanoic acid hydrate is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological and metabolic disorders. Its chiral structure makes it valuable in the production of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. Additionally, it is employed in peptide synthesis, where its unique cyclohexyl group contributes to the stability and specificity of peptide-based therapeutics. This compound is also explored in the study of enzyme inhibitors, aiding in the development of treatments for conditions such as diabetes and cancer.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,655.00
inventory 250mg
10-20 days ฿396.00
inventory 1g
10-20 days ฿819.00
inventory 10g
10-20 days ฿4,320.00

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(S)-2-Amino-3-cyclohexylpropanoic acid hydrate
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(S)-2-Amino-3-cyclohexylpropanoic acid hydrate is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological and metabolic disorders. Its chiral structure makes it valuable in the production of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. Additionally, it is employed in peptide synthesis, where its unique cyclohexyl group

(S)-2-Amino-3-cyclohexylpropanoic acid hydrate is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological and metabolic disorders. Its chiral structure makes it valuable in the production of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. Additionally, it is employed in peptide synthesis, where its unique cyclohexyl group contributes to the stability and specificity of peptide-based therapeutics. This compound is also explored in the study of enzyme inhibitors, aiding in the development of treatments for conditions such as diabetes and cancer.

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