2-Amino-3-(2-fluoro-4,5-dihydroxyphenyl)propanoic acid

95%

Reagent Code: #137787
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CAS Number 102034-49-1

science Other reagents with same CAS 102034-49-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.18 g/mol
Formula C₉H₁₀FNO₄
badge Registry Numbers
MDL Number MFCD00274040
thermostat Physical Properties
Melting Point 202-208 °C
Boiling Point 465.3±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.553±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in biochemical research as a tyrosine analog to study enzyme mechanisms, particularly in kinases and hydroxylases. Its fluorinated aromatic ring allows for probing electronic and steric effects in protein binding sites. Also employed in the synthesis of modified peptides to investigate structure-activity relationships. Shows potential in developing enzyme inhibitors due to its altered hydroxylation pattern.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Light Gray to Dark Brown Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿20,600.00
250mg
10-20 days ฿34,350.00
1g
10-20 days ฿68,660.00
2-Amino-3-(2-fluoro-4,5-dihydroxyphenyl)propanoic acid
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Used in biochemical research as a tyrosine analog to study enzyme mechanisms, particularly in kinases and hydroxylases. Its fluorinated aromatic ring allows for probing electronic and steric effects in protein binding sites. Also employed in the synthesis of modified peptides to investigate structure-activity relationships. Shows potential in developing enzyme inhibitors due to its altered hydroxylation pattern.

Used in biochemical research as a tyrosine analog to study enzyme mechanisms, particularly in kinases and hydroxylases. Its fluorinated aromatic ring allows for probing electronic and steric effects in protein binding sites. Also employed in the synthesis of modified peptides to investigate structure-activity relationships. Shows potential in developing enzyme inhibitors due to its altered hydroxylation pattern.

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