(R)-3-Amino-3-(3-cyanophenyl)propanoic acid

≥98%

Reagent Code: #229539
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CAS Number 761396-82-1

science Other reagents with same CAS 761396-82-1

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scatter_plot Molecular Information
Weight 190.2 g/mol
Formula C₁₀H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD04113655
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antidiabetic drugs such as DPP-4 inhibitors. Its structural configuration enables high selectivity and potency in drug formulations. The presence of both amino and carboxylic acid functional groups allows for peptide coupling and derivatization, making it valuable in medicinal chemistry for building complex bioactive molecules. Also employed in the preparation of enzyme inhibitors due to its ability to mimic natural amino acid substrates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,320.00
inventory 250mg
10-20 days ฿9,030.00
inventory 1g
10-20 days ฿22,180.00

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(R)-3-Amino-3-(3-cyanophenyl)propanoic acid
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antidiabetic drugs such as DPP-4 inhibitors. Its structural configuration enables high selectivity and potency in drug formulations. The presence of both amino and carboxylic acid functional groups allows for peptide coupling and derivatization, making it valuable in medicinal chemistry for building complex bioactive molecules. Also employed in the preparation of enzyme inhibitors due to its ab

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antidiabetic drugs such as DPP-4 inhibitors. Its structural configuration enables high selectivity and potency in drug formulations. The presence of both amino and carboxylic acid functional groups allows for peptide coupling and derivatization, making it valuable in medicinal chemistry for building complex bioactive molecules. Also employed in the preparation of enzyme inhibitors due to its ability to mimic natural amino acid substrates.

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