4-Chlorophenylalaninol Hydrochloride

≥97%

Reagent Code: #171700
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CAS Number 1379971-06-8

science Other reagents with same CAS 1379971-06-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.11 g/mol
Formula C₉H₁₃Cl₂NO
badge Registry Numbers
MDL Number MFCD08454680
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its structure supports the creation of stereoselective compounds, making it valuable in medicinal chemistry research. Commonly employed in the preparation of peptidomimetics and receptor ligands due to its amino alcohol and aromatic halide functionality. Also utilized in asymmetric synthesis for catalyst design and in the study of metabolic pathways involving phenylalanine derivatives.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,500.00
inventory 5g
10-20 days ฿22,080.00

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4-Chlorophenylalaninol Hydrochloride
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Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its structure supports the creation of stereoselective compounds, making it valuable in medicinal chemistry research. Commonly employed in the preparation of peptidomimetics and receptor ligands due to its amino alcohol and aromatic halide functionality. Also utilized in asymmetric synthesis for catalyst design and in the study of metabolic pathways invol

Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its structure supports the creation of stereoselective compounds, making it valuable in medicinal chemistry research. Commonly employed in the preparation of peptidomimetics and receptor ligands due to its amino alcohol and aromatic halide functionality. Also utilized in asymmetric synthesis for catalyst design and in the study of metabolic pathways involving phenylalanine derivatives.

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