2-amino-3-(2,6-dimethylphenyl)propanoic acid

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Reagent Code: #137856
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CAS Number 132466-22-9

science Other reagents with same CAS 132466-22-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.24 g/mol
Formula C₁₁H₁₅NO₂
badge Registry Numbers
MDL Number MFCD02684448
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

2-Amino-3-(2,6-dimethylphenyl)propanoic acid is a chiral, unnatural α-amino acid used as a key building block and intermediate in pharmaceutical research and synthesis. Its bulky, hydrophobic 2,6-dimethylphenyl side chain imparts steric hindrance and specific interactions, making it valuable for designing peptides, peptidomimetics, and small-molecule drugs. It supports the development of enzyme inhibitors, receptor ligands, and bioactive compounds with potential applications in local anesthetics, anti-inflammatory agents, and central nervous system therapeutics. The compound's chirality enables asymmetric synthesis for producing enantiomerically pure pharmaceuticals.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,300.00
inventory 1g
10-20 days ฿2,600.00
inventory 5g
10-20 days ฿9,100.00

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2-amino-3-(2,6-dimethylphenyl)propanoic acid
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2-Amino-3-(2,6-dimethylphenyl)propanoic acid is a chiral, unnatural α-amino acid used as a key building block and intermediate in pharmaceutical research and synthesis. Its bulky, hydrophobic 2,6-dimethylphenyl side chain imparts steric hindrance and specific interactions, making it valuable for designing peptides, peptidomimetics, and small-molecule drugs. It supports the development of enzyme inhibitors, receptor ligands, and bioactive compounds with potential applications in local anesthetics, anti-in

2-Amino-3-(2,6-dimethylphenyl)propanoic acid is a chiral, unnatural α-amino acid used as a key building block and intermediate in pharmaceutical research and synthesis. Its bulky, hydrophobic 2,6-dimethylphenyl side chain imparts steric hindrance and specific interactions, making it valuable for designing peptides, peptidomimetics, and small-molecule drugs. It supports the development of enzyme inhibitors, receptor ligands, and bioactive compounds with potential applications in local anesthetics, anti-inflammatory agents, and central nervous system therapeutics. The compound's chirality enables asymmetric synthesis for producing enantiomerically pure pharmaceuticals.

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