4-Nitro-DL-phenylalanine monohydrate

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Reagent Code: #216792
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Alias 4-Nitro-DL-phenylalanine monohydrate
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CAS Number 2922-40-9

science Other reagents with same CAS 2922-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.19 g/mol
Formula C₉H₁₀N₂O₄·H₂O
badge Registry Numbers
EC Number 220-868-6
MDL Number MFCD00007384
thermostat Physical Properties
Melting Point 236-237 °C(dec.)(lit.)
Boiling Point 414.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.408 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis and pharmaceutical research as a chiral building block for the preparation of bioactive molecules. Serves as an intermediate in the development of enzyme inhibitors and antimicrobial agents. Its nitro-aromatic structure allows for further functionalization through reduction and coupling reactions, making it valuable in medicinal chemistry for designing peptide analogs and studying structure-activity relationships. Also employed in biochemical studies to probe amino acid metabolism and enzyme specificity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿470.00
25g
10-20 days ฿1,940.00
4-Nitro-DL-phenylalanine monohydrate
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Used in organic synthesis and pharmaceutical research as a chiral building block for the preparation of bioactive molecules. Serves as an intermediate in the development of enzyme inhibitors and antimicrobial agents. Its nitro-aromatic structure allows for further functionalization through reduction and coupling reactions, making it valuable in medicinal chemistry for designing peptide analogs and studying structure-activity relationships. Also employed in biochemical studies to probe amino acid metaboli

Used in organic synthesis and pharmaceutical research as a chiral building block for the preparation of bioactive molecules. Serves as an intermediate in the development of enzyme inhibitors and antimicrobial agents. Its nitro-aromatic structure allows for further functionalization through reduction and coupling reactions, making it valuable in medicinal chemistry for designing peptide analogs and studying structure-activity relationships. Also employed in biochemical studies to probe amino acid metabolism and enzyme specificity.

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